McDonald's(R) USA Voluntarily Recalls Shrek Forever After(TM) Glassware

/PRNewswire/ -- In collaboration with the Consumer Product Safety Commission (CPSC), and as a precautionary measure, McDonald's USA today issued a voluntary recall of its four Shrek Forever After(TM) glassware recently offered in its U.S. restaurants. Customers should stop using the glasses and visit www.mcdonalds.com/glasses beginning June 8 for instructions on how to return them and get a refund.

McDonald's safety standards are among the highest in the industry and the company has a strong track record. To be clear, the glassware was evaluated by an independent third-party laboratory which is accredited by the CPSC, and determined to be in compliance with all applicable federal and state requirements at the time of manufacture and distribution. However, in light of the CPSC's evolving assessment of standards for cadmium in consumer products, McDonald's determined in an abundance of caution that a voluntary recall of the Shrek Forever After glasses is appropriate.

"When the U.S. Consumer Product Safety Commission approached McDonald's about cadmium in their current movie-themed drinking glasses, the company responded quickly, agreed to cooperate fully and acted on the side of caution," said Scott Wolfson, Director of the Office of Information and Public Affairs, CPSC. "The glasses have far less cadmium than the children's metal jewelry that CPSC has previously recalled."

McDonald's has a longstanding, cooperative relationship with the CPSC, and continues to follow their lead as testing protocols and new scientific information becomes available.

The Shrek Forever After glassware was offered in four glass designs at McDonald's restaurants beginning May 21. The four designs include Puss n' Boots, Shrek, Princess Fiona and Donkey. Customers can get instructions to return the glassware and request a refund by visiting www.mcdonalds.com/glasses beginning June 8. Customers can also call McDonald's toll-free number at 1-800-244-6227. Previous McDonald's promotional glassware is not involved in the recall.

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Chesley: Toyota Apologies Are Not Getting Dangerous Cars Off Roads

/PRNewswire/ -- With the latest news that Toyota may recall its 2009 and 2010 Corollas because of power steering defects, Toyota has now admitted to defects in its vehicles' accelerator, braking and steering systems - the three most important aspects of operating a motor vehicle.

Stanley M. Chesley of the Cincinnati-based law firm of Waite, Schneider, Bayless & Chesley Co., L.P.A. - whose firm has filed a major RICO class action against Toyota for deceiving its customers and dealers about these mounting defects - stated that "when your Toyota's accelerator, brakes and steering are all defective, what you really have is a failure of your car's electronic controls, which function as the car's brain and central nervous system."

Congressman Bart Stupak recently amplified Chesley's suspicion, noting that Toyota's internal documents made clear that, as far back as 2002, Toyota was aware that electronic control system problems may be causing sudden acceleration. Despite this Congressional investigation, however, Toyota continues to bar investigators from examining its electronic control technology.

Now, with Toyota's recall of a staggering 11 million vehicles, Toyota's president and CEO, Akio Toyoda, yesterday indicated that he won't come to the U.S. to testify at upcoming congressional hearings on the recalls.

Chesley stated, "No one is above the law. Presidents of tobacco companies, and even U.S. Presidents, have testified before congressional committees. Akio Toyoda's grand apologies from 6,000 miles away don't release him from appearing before Congress and they don't explain Toyota's nearly decade-long cover up of these defects."

According to news sources, Toyota's faulty engineering and sloppy quality control - all of which stem from decision-making at Toyota's Japanese headquarters - have caused at least 39 confirmed deaths, countless injuries and billions of dollars in economic damage to Toyota drivers. As Chesley remarked, "for Toyota's CEO to even consider refusing to appear before Congress, particularly when he's looking to the United States to make Toyota the world's largest car manufacturer, is outrageous."

Chesley filed the RICO class action, in part, because the evidence continues to disprove Toyota's statements about the defects' causes. All of this evidence highlighting Toyota's deception underscores the company's pattern of corrupt and fraudulent practices, which is what RICO, the federal racketeering statute, prohibits.

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TYLENOL Recall Confirms Congress, FDA Must Regulate Wood Pallets to Prevent Threats to U.S. Food, Drug Supply

/PRNewswire/ -- The expanded recall of TYLENOL Arthritis pain reliever is fresh evidence of the need for Congress and the FDA to regulate wood pallets used to transport food and pharmaceuticals in the United States because of the dangers they pose to human health.

The move earlier this week by McNeil Consumer Healthcare and FDA to expand the voluntary recall to include all lots of TYLENOL Arthritis Pain Caplet 100 count bottles comes on the heels of independent scientific studies showing wood pallets harbor deadly food poisoning bacteria and pathogens.

"How much more evidence does Congress and the FDA need? The TYLENOL recall proves wooden pallet shipping platforms are a dangerous threat to the pharmaceuticals we depend on, while recent independent studies we've commissioned in four cities demonstrate the dangers they pose to our food supply," said Bob Moore, Chairman & CEO, Intelligent Global Pooling Systems (iGPS Company LLC).

"The one to two billion wood pallets in circulation in the United States are the common denominator in the supply chain - practically every product we ingest is shipped on a wood pallet. Congress and FDA cannot afford to overlook them any longer as they consider ways to strengthen our national food safety law."

Chemicals used to treat wood pallets were cited as causing a moldy, musty or mildew-like odor in the TYLENOL product that caused nausea, vomiting, diarrhea and stomach pain in consumers. Wood pallets made with "engineered wood" components also contain urea formaldehyde - a known carcinogen - which may come into contact with food under a variety of scenarios when it is stored and shipped on wooden pallets. Formaldehyde is also released into the air when it off-gases from pallets in storage and transportation compartments, posing a risk to the health of workers and consumers.

Wood pallets pose other dangerous risks to food safety. Wood pallets are susceptible to insect infestation and require heat treatment or fumigation before they can be moved cross-border. Fumigation is often performed with methyl bromide, a highly toxic, ozone-depleting chemical. Rusty nails and wood shards that can penetrate food packaging are also a risk.

Recent tests commissioned by iGPS have found Salmonella, E. coli, Listeria and extremely high bacteria counts on scores of wood pallets pulled at random from pallet depots in Washington, DC, Baltimore, Philadelphia and Portland, ME. Listeriosis is responsible for approximately 2,500 illnesses and 500 deaths in the United States annually and is the leading cause of death among food borne bacterial pathogens, with fatality rates exceeding even Salmonella and Clostridium Botulinum.

The iGPS test results are consistent with similar findings by USDA and FDA. A new USDA study found salmonella-causing bacteria can be harbored on wooden shelving carts used for transporting eggs into processing plants. The FDA has also drawn attention to the health risks that wood pallets present. According to the FDA's Guidance for Industry: Control of Listeria monocytogenes in Refrigerated or Frozen Ready-To-Eat Foods (February, 2008), "In areas where RF-RTE [refrigerated-ready to eat] foods are processed or exposed, we recommend that you use pallets that can be easily cleaned and keep them in good condition, and that you not use wood pallets in areas where RF-RTE foods are processed or exposed or in other areas for wet processing and storage."

A trip to virtually any wood pallet depot reveals thousands of wood pallets stacked outdoors, sitting in mud and water-logged (some even serving as nests for rodents) -- a clear violation of industry "best practices" calling for wood pallets to be stored in dry indoor locations.

"This is an industry that openly ignores its own safety rules and transports our food supply on deplorably unsanitary platforms," said Moore. "We call on Congress and the FDA to take a comprehensive look at the role wood pallets play in contaminating our food and drug supplies - and to take action."

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CPSC, Goodman Manufacturing Co. Announce Changes to 1998 Recall Program to Replace Dangerous Home Heating Vent Pipes

/PRNewswire/ -- The CPSC and Goodman Manufacturing Company, of Houston, TX, are urging consumers who have not yet responded to the previously-announced 1998 recall to do so immediately. After October 1, 2009, the remedy consumers receive will change to be identical to modifications recently announced for a related recall.

The recall included about 10,000 Plexvent and Ultravent HTPV pipe systems attached to certain Goodman mid-efficiency furnaces manufactured from October 1988 to July 1994 (models GUP, GDP, GUPS, GDPS, GUPI, GDPI, GUPX, GDPX, GMP and GMPV for the following brands manufactured by Goodman: Janitrol, GMC, Hamilton Electric, Franklin, Liberty and Sears/Kenmore). The HTPV pipe used for these vents could be susceptible to corrosion, cracking and joint separation, which could result in the release of carbon monoxide (CO) into living areas, posing a danger to consumers. Goodman did not manufacture the HTPV pipe.

The following table describes the different remedies available to consumers with qualifying furnaces that use the two leading brands of HTPV pipe - Plexvent and Ultravent.

Plexvent Owners Ultravent Owners
--------------- ----------------

Valid claims Will receive:
initiated on or -- a new, professionally-installed venting
before October 1, system free of charge
2009, with
remediation or
completed and
required -- a new, high-efficiency Goodman furnace and
documentation suitable vent for the manufacturer's price
submitted by (of just the furnace), with no charge for
January 1, 2010. labor, associated materials or dealer markup.

---------------------- ----------------------- --------------------------

Valid claims A rebate up to $400 A rebate up to $250
initiated toward either an HTPV toward either an HTPV
after October 1, 2009 replacement system, or replacement
a new, high-efficiency system, or a new,
furnace from Goodman high-efficiency furnace
that does not require from Goodman that does HTPV. not require HTPV.

---------------------- ----------------------- --------------------------


Consumers who register after October 1, 2009 and who choose to repair their systems will be responsible for up-front payment of parts, labor and permits, and will be responsible for arranging to have the work performed.

Consumers should determine whether they have a recalled HTPV pipe system by checking the vent pipes attached to their natural gas furnace. Vent pipes subject to this recall can be identified as follows:

-- the vent pipes are plastic;
-- the vent pipes are colored gray or black;
-- "Plexvent," "Plexvent II" or "Ultravent" is stamped on the vent pipe
or printed on stickers placed on pieces used to connect the vent
pipes; and

-- the vent pipes are located on furnaces and the pipes go through the
sidewalls of structures.


Other plastic vent pipes, such as white PVC, are not included in the recall.

Owners of Goodman furnaces that are vented with HTPV pipe should immediately call Goodman at (800) 394-8084 from 8 a.m. to 5 p.m. CT Monday through Friday. CPSC reminds all consumers to have fuel-burning appliances professionally inspected each year to check for cracks or separations in the vents that could allow CO to leak into the home. In addition, CPSC recommends that every home should have at least one CO alarm.

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How Dangerous Is Hydroxycut?

/24-7/ -- On May 1, 2009, the US Food and Drug Administration (FDA) issued a press release urging consumers to stop using 14 varieties of the diet aid Hydroxycut and return unused portions to the place of purchase. The FDA also sent a letter to health care professionals stating that officials "believe [Hydroxycut] presents a serious public health risk." In response, the manufacturer of Hydroxycut, Iovate Health Sciences, Inc., decided to issue a voluntary recall of all products named by the FDA. But just how dangerous is Hydroxycut, really? Was the FDA justified in its action, or is this an overhasty response to a minor health concern.

About Hydroxycut Injuries

The main rationale for the FDA's action regarding Hydroxycut is liver damage. In some patients it seems to create acute liver toxicity that required hospitalization in more than 2/3 of the reported cases, and required liver transplants for two of them. One of the patients was deemed unsuitable for a liver transplant because of significant damage to other organs. This patient, a 17-year old male, had taken an elevated dose of Hydroxycut, and died after the decision was made not to pursue the liver transplant.

In addition to liver damage, the FDA determined that a number of serious illnesses have been associated with Hydroxycut use, including cardiovascular injury, seizures, and severe muscle damage known as rhabdomyolysis.

The Numbers of Hydroxycut Injuries

In its press releases and statements, the FDA claims there have been 23 cases of confirmed liver damage resulting from the use of Hydroxycut. The cases appeared over a seven year period. With millions of bottles of Hydroxycut being sold every year, the number of injuries may seem very small, making many believe that FDA's statement and subsequent recall is something of an overreaction.

The Rationale for the Hydroxycut Action

Hydroxycut seems to cause what is known as idiosyncratic liver toxicity, a condition which is inherently very rare. The toxic reaction occurs in less than 10 people per 100,000, and often in less than 1 per 100,000. Although toxic reactions are rare, idiosyncratic liver toxicity is the most common form of drug-induced liver toxicity because it is unpredictable, generally undetected in clinical trials, and often occurs with only recommended doses of a drug.

In addition, the FDA did not know what ingredient of Hydroxycut was responsible for the liver toxicity. It did not know whether liver toxicity was the result of a biologic extract or a heavy metal. It did not even know whether the toxicity may have been the result of contaminated or badly blended pills. Reports of liver damage have been associated with Hydroxycut since its introduction, but it was believed at first that the ingredient ephedra, associated with seizure, cardiovascular damage, and other adverse health effects, was responsible for the damage. But Hydroxycut has been ephedra-free since the ingredient was banned in 2004, and reports of liver damage have continued.

Because of all the unknowns, the FDA could not issue a specific caution that would identify users with an elevated risk from Hydroxycut and thereby reduce future cases of liver toxicity. The only way the FDA could protect users was to ask them to stop using Hydroxycut, a request that will likely stay in effect until a causative agent can be identified.

So, How Dangerous Is Hydroxycut?

We're back to the place we started then, with the question of how dangerous is this diet aid? The answer is: no-one knows. The FDA's action is designed to stop more people from suffering adverse, potentially deadly reactions to Hydroxycut while the agency and the manufacturer of the supplement determine what is the cause. Once the ingredient responsible has been identified, we can expect Hydroxycut to return to the market either reformulated or with specific warnings that may help users make informed decisions about whether a diet supplement with no proven effectiveness is worth the potential risk.

If you would like to learn more about Hydroxycut or other dangerous drugs, visit the website of pharmaceutical injury law firm Schlichter, Bogard & Denton today.

Source: Schlichter, Bogard & Denton

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Pistachio Growers and Processors Announce New Web Site to Inform Consumers, Retailers of Safe Pistachio Brands

TT Note: This new web site is a great idea. We've not been purchasing pistachios due to the recent salmonella scare. Perhaps this site will keep this industry from being almost completely destroyed unlike the recent peanut issues.

/PRNewswire/ -- As part of ongoing collaboration with the United States Food and Drug Administration (FDA), pistachio growers and processors today announced a new Web site - www.pistachiorecall.org - that lists specific pistachio products and brands that are confirmed safe to consume.

The Web site is produced by CAL-PURE, a co-op of California pistachio growers ("CAL-PURE"), and the Western Pistachio Association ("WPA") and is accessible directly and via a link on the FDA Web site at www.fda.gov/pistachios. The new site is being made available in light of a pistachio recall by the processor, Setton Pistachio of Terra Bella, Inc. and Setton International, due to potential Salmonella contamination. The recall action has been taken on a precautionary basis, and the FDA reports no illnesses tied to the recalled pistachios.

Only pistachios processed by the Setton Pistachio and Setton International facilities are affected by the recall measures, and the majority of processors, pistachio products and foods containing pistachio products are not involved with the recall. The new Web site, www.pistachiorecall.org, will be updated on an ongoing basis to ensure consumers have access to the latest, most accurate information available related to safe products.

The health and safety of consumers is the pistachio growers and processors number-one priority and, as such, CAL-PURE and the WPA are committed to continuing to work closely with regulators and industry leaders to address questions about pistachio safety. The pistachio community is dedicated to providing a safe, wholesome product and is eager to quickly put any concerns to rest so that consumers can enjoy pistachios and pistachio products with confidence.

For additional details about the Setton Pistachio recall, consumers may also visit www.fda.gov/pistachios for the latest information, as well as products that are affected by the voluntary recall. The FDA site also provides updates on the status of the recall, which as of today, includes the following revised statement:

"FDA is advising consumers not to eat pistachios or food products containing them (such as pistachio bakery goods and pistachio ice cream) unless they can determine that the products do not contain pistachios from Setton Pistachio of Terra Bella Inc. The FDA consumer alert is available at this link: http://www.fda.gov/bbs/topics/NEWS/2009/NEW01982.html."

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ALDI Statement Regarding Peanut Butter Products Recall

ALDI has two suppliers who manufacture the Cambridge cheese crackers with peanut butter, one of which is Kellogg's. As a precautionary measure, as of Jan. 15 ALDI and Kellogg's voluntarily recalled the Kellogg-produced peanut butter crackers due to industry reports of salmonella at affiliated plants, though no illnesses have been reported regarding these Kellogg-manufactured products. The second manufacturer of our cheese crackers with peanut butter does not use the peanut plant where the salmonella outbreak was reported. However, as a further precautionary measure, as of Jan.20 ALDI has recalled the additional Cambridge cheese crackers with peanut butter as well as our Grandessa peanut butter cookies.

To tell the difference between the two manufacturers of Cambridge cheese crackers with peanut butter, customers should look at the net weight on the front of the package of crackers. A net weight of 7.44 oz (210 grams) was produced by Kellogg's while a net weight of 7 1/3 oz (208 grams) was produced by our second manufacturer.

All other ALDI peanut products or products that contain peanuts or a peanut paste have not been the subject of concern regarding potential salmonella poisoning.

Salmonella is an organism that can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis. For more information on Salmonella, please visit the Centers for Disease Control and Prevention's Web site at http://www.cdc.gov.

Consumers who have purchased the recalled products are urged to return them, regardless of the manufacturer, to receive a refund. ALDI Consumer Affairs may be reached at 630-761-2740.

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Peanut Corporation of America Expands Nationwide Recall of Peanut Butter

Peanut Corporation of America (PCA), is expanding the recall of peanut butter and voluntarily recalling peanut paste made at its Blakely, Georgia facility because the products have the potential to be contaminated with Salmonella. Salmonella is an organism that can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.

The recalled peanut butter and peanut paste were distributed to institutions, food service industries, and private label food companies in 24 states, the province of Saskatchewan in Canada, Korea and Haiti. The U.S. states are the following: Arkansas, California, Colorado, Florida, Georgia, Illinois, Indiana, Iowa, Maryland, Michigan, Minnesota, Missouri, Nevada, New Hampshire, New Jersey, New York, North Carolina, Ohio, Pennsylvania, South Carolina, Tennessee, Texas, Utah and Virginia. In addition, affected product was used as an ingredient in other products that may have been distributed in other states.

None of the peanut butter being recalled is sold directly to consumers through retail stores by PCA.

The recalled peanut butter in the expanded recall is sold by PCA in bulk packaging in containers ranging in size from five to 1,700 pounds. The peanut paste is sold in sizes ranging from 35-pound containers to tanker containers. The lot numbers for all recalled products are at the end of this news release. All of the peanut butter and peanut paste in the expanded recall was made on or after July 1, 2008, and only at the Georgia facility.

The potential for contamination was noted after a small number of samples from unopened containers and environmental samples from the Blakely, Georgia facility tested positive for Salmonella. The U.S. Food and Drug Administration has said the investigation is "very active and dynamic," and PCA continues to work closely with the FDA and the Centers for Disease Control and Prevention as they continue their investigation into the nationwide outbreak of Salmonella.

The Blakely, Georgia facility has currently stopped producing all products as the FDA and CDC continue their investigation, but some PCA staff remain to assist in the on-going investigation.

PCA is notifying customers that may have received the recalled product by phone and/or in writing. Customers should segregate and hold the product and call PCA at 1-877-564-7080 for further instructions. "We deeply regret that this product recall has expanded, and our first priority is to protect the health of our customers," said Stewart Parnell, President of Peanut Corporation of America.

The following is a list of all the products affected by the original recall and the amended recall:

PCA Stock # Pack Size Description Affected:

551000 6 ct / 5 lb Creamy Stabilized Peanut Butter

551000 AZ 6 ct / 5 lb Creamy Stabilized Peanut Butter with Sugar

551006 6 ct / 5 lb Crunchy Stabilized Peanut Butter

551020 35 lb Creamy Stabilized Peanut Butter

551022 35 lb Natural Course Peanut Paste

551025 35 lb Old Fashioned Creamy Peanut Butter w/ 1% Salt

551026 35 lb Old Fashioned Crunchy Peanut Butter w/ 1% Salt

551034 35 lb Crunchy Stabilized Peanut Butter

551035 35 lb Crunchy Natural Peanut Butter

551040 35 lb Creamy Natural Peanut Butter

551049 50 lb Sugar Free Creamy Stabilized Peanut Butter

551050 50 lb Creamy Stabilized Peanut Butter

551050-PO 50 lb Creamy Stabilized Peanut Butter with Palm Oil

551050-D 50 lb Dark Creamy Stabilized Peanut Butter

551050-XS 50 lb Creamy Extra Stabilized Peanut Butter

551051 50 lb Creamy Stabilized Peanut Butter with Monodiglyceride

551053 50 lb Crunchy Stabilized Peanut Butter

551053-OS 50 lb Extra Crunchy Stabilized Peanut Butter

551059 475 lb Creamy Natural Peanut Butter with Stabilizer

551060 35 lb Organic Natural Creamy Peanut Butter

551061 35 lb Organic Old Fashioned Crunchy Peanut Butter

551062 35 lb Organic Crunchy Natural Peanut Butter

551063 35 lb Organic Old Fashioned Creamy Peanut Butter

551064 35 lb Organic Natural Creamy Peanut Butter

551072 45 lb Peanut Butter Variegate

551080 475 lb Creamy Natural Redskin Peanut Butter with Salt

551082 475 lb Creamy Natural Peanut Butter

551082-DR 475 lb Dark Roasted Creamy Natural Peanut Butter

561000 35 lb Pet Food Paste

561000 475 lb Feed Grade Peanut Butter

100TPASTE 1700 lb Creamy Natural Peanut Butter

RM-PASTE 1700 lb Peanut Paste

Lot Numbers Affected:

8183 8184 8185 8186 8187 8188 8189 8190 8191 8192 8193 8194 8195 8196 8197 8198
8199 8200 8201 8202 8203 8204 8205 8206 8207 8208 8209 8210 8211 8212 8213 8214
8215 8216 8217 8218 8219 8220 8221 8222 8223 8224 8225 8226 8227 8228 8229 8230
8231 8232 8233 8234 8235 8236 8237 8238 8239 8240 8241 8242 8243 8244 8245 8246
8247 8248 8249 8250 8251 8252 8253 8254 8255 8256 8257 8258 8259 8260 8261 8262
8263 8264 8265 8266 8267 8268 8269 8270 8271 8272 8273 8274 8275 8276 8277 8278
8279 8280 8281 8282 8283 8284 8285 8286 8287 8288 8289 8290 8291 8292 8293 8294
8295 8296 8297 8298 8299 8300 8301 8302 8303 8304 8305 8306 8307 8308 8309 8310
8311 8312 8313 8314 8315 8316 8317 8318 8319 8320 8321 8322 8323 8324 8325 8326
8327 8328 8329 8330 8331 8332 8333 8334 8335 8336 8337 8338 8339 8340 8341 8342
8343 8344 8345 8346 8347 8348 8349 8350 8351 8352 8353 8354 8355 8356 8357 8358
8359 8360 8361 8362 8363 8364 8365 8366 9001 9002 9003 9004 9005 9006 9007 9008
9009 9010 9011 9012 9013 9014 9015 9016

PCA Stock # Pack Size Description Affected:

561058 Tanker Coarse Natural Paste

Lot Numbers Affected:
8169 8170 8172 8173 8174 8184 8185 8186 8187 8203 8204 8205 8206 8214 8215 8216
8217 8219 8220 8221 8222 8223 8225 8226 8227 8228 8259 8260 8261 8262 8263 8264
8280 8281 8282 8283 8302 8303 8304 8305 8308 8309 8310 8311 8343 8344 8345 8346
8347 8350 8351 8352

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CPSC, Manufacturers Announce Changes to 1998 Recall Program to Replace Dangerous Home Heating Vent Pipes Remedy Changes for Registrations after May 1

The U.S. Consumer Product Safety Commission (CPSC) and various home heating furnace, boiler, and high-temperature plastic vent (HTPV) manufacturers are urging home owners who have not yet responded to the previously-announced 1998 recall, to do so immediately. After May 1, 2009, the remedy consumers receive under the existing program, which has been operating continuously for almost 11 years, will change.

The recall, first announced in February 1998, included about 250,000 Plexvent and Ultravent HTPV pipe systems attached to gas or propane furnaces and boilers in homes. The HTPV pipes can crack or separate at the joints and leak deadly carbon monoxide (CO) gas. The following table includes the different remedies available to consumers with qualifying heating systems vented with two leading brands of HTPV pipe - Plexvent and Ultravent.

For valid claims initiated on or before May 1, 2009, with remediation completed and required documentation submitted by October 1, 2009: Plexvent owners will receive a new, professionally-installed venting system free of charge or a rebate up to $$400 towards purchase of a new, high-efficiency appliance from the same manufacturer that does not require HTPV. Ultravent owners will receive a new, professionally-installed venting system for about $$250 or a rebate of $$250 towards purchase of a new, high-efficiency appliance from the same manufacturer that does not require HTPV.

For valid claims initiated after May 1, 2009: Plexvent owners will receive a rebate up to $$400 toward either an HTPV replacement system, or a new, high-efficiency appliance from the same manufacturer that does not require HTPV. Ultravent owners will receive a rebate up to $$250 toward either an HTPV replacement system, or a new, high-efficiency appliance from the same manufacturer that does not require HTPV.

Consumers who register after May 1, 2009 and who choose to repair their systems will be responsible for up-front payment of parts, labor and permits, and will be responsible for arranging to have the work performed.

Consumers should determine whether they have a recalled HTPV pipe system by checking the vent pipes attached to their natural gas or propane furnace or boiler. Vent pipes subject to this recall can be identified as follows:

the vent pipes are plastic;

the vent pipes are colored gray or black;

"Plexvent," "Plexvent II" or "Ultravent" is stamped on the vent pipe or printed on stickers placed on pieces used to connect the vent pipes; and

the vent pipes are located on furnaces (and the pipes go through the sidewalls of structures) or on boilers.

Other plastic vent pipes, such as white PVC, are not included in the recall.

After checking the vent pipes, consumers should call (800) 758-3688 between 8 a.m. and 7 p.m. ET Monday through Friday to sign up for HTPV pipe system replacement. The following manufacturers are participating in this program:

Armstrong Air Conditioning Inc., Bard Manufacturing Co., Burnham Corp., Dunkirk Radiator Corp., Evcon Industries Inc., Heat Controller Inc., International Comfort Prod. Corp.(USA), Lennox Industries Inc., Nordyne Inc., Peerless Heater Co., Pennco Inc., Plexco Inc., Raypak Inc., Rheem Manufacturing Co., Slant/Fin Corp., The Trane Co., Trianco-Heatmaker Inc., Utica Boilers Inc., Vaillant Corp., Weil-McLain, Westcast Inc., York International Corp.York International Corp.

CPSC reminds all consumers to have fuel-burning appliances professionally inspected each year to check for cracks or separations in the vents that could allow CO to leak into the home. In addition, CPSC recommends that every home should have at least one CO alarm.

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Lance Sandwich Crackers NOT Impacted by Recent Peanut Butter Recall

(BUSINESS WIRE)--In response to a growing number of consumer inquiries, Lance, Inc. released the following statement about its sandwich crackers containing peanut butter.

No Lance sandwich crackers containing peanut butter are affected by this week’s recent peanut butter recall. In fact, all Lance, Inc. information and recent testing reinforce that there is no concern with the quality or safety of peanut butter used in Lance sandwich crackers.

Based on this week’s news, the Food Safety Division of the North Carolina Department of Agriculture visited Lance’s Charlotte, N.C., bakery yesterday. After reviewing the Lance food safety programs and records specific to peanut butter, Lance was given a clean bill of health.

Lance manufactures 100% of the peanut butter used in its sandwich crackers and does not receive peanut butter from the supplier involved in the recall.

Lance enforces a very stringent food safety program with the raw ingredients and final product coming in and out of Lance facilities -- particularly with peanut butter. Lance regularly conducts extensive microbial testing of its peanut butter to ensure only high-quality, safe food ingredients are used.

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Johnson and Johnson--Merck Consumer Pharmaceuticals Company Announces Urgent Voluntary Nationwide Recall Of Infants' Mylicon Gas Relief Dye Free Drops

Johnson & Johnson • Merck Consumer Pharmaceuticals Company (JJMCP) is voluntarily recalling approximately 12,000 units of Infants' MYLICON® GAS RELIEF DYE FREE drops (simethicone-antigas) non-staining sold in 1 oz. plastic bottles that were distributed after October 5, 2008 nationwide. The company is taking this action in consultation with the U.S. Food and Drug Administration (FDA). Although the potential for serious medical events is low, the company is implementing this recall to the consumer level as a precaution after determining that some bottles could include metal fragments that were generated during the manufacturing process. If any medical events were to occur, most are expected to be temporary and resolve without medical treatment. Parents who have given the product to their infant and are concerned should contact their health care provider immediately.

The two lots of Infants' MYLICON® GAS RELIEF DYE FREE drops non-staining 1 oz. bottles included in the recall are:

71683791111-1
Lot SMF007
Exp 09/10
Infants' Mylicon® Gas Relief Dye Free Non-Staining Drops 1 oz.

71683791111-1
Lot SMF008
Exp 09/10
Infants' Mylicon® Gas Relief Dye Free Non-Staining Drops 1 oz.

Consumers can find the lot numbers on the bottom of the box containing the product and also on the lower left side of the sticker on the product bottle.

Consumers who purchased Infants' MYLICON® GAS RELIEF DYE FREE drops non-staining included in this recall should immediately stop using the product and contact the company at 1-800-222-9435 (Monday – Friday, 8:00 a.m. – 8:00 p.m. EST) or via the internet at www.mylicon.com for instructions regarding how to dispose of the product and request a replacement or refund.

Infants' MYLICON® drops are sold over-the counter, in retail stores and pharmacies, as an anti-gas medicine to relieve the discomfort of infant gas frequently caused by air swallowing or by certain formulas or foods.

The recall does not affect any Original Infants' MYLICON® GAS RELIEF products (1/2 oz. or 1 oz. size) or Infants' MYLICON® GAS RELIEF DYE FREE drops non-staining (1/2 oz. size).

The manufacturer has instructed retailers and wholesalers to return their inventories.

Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

Online: www.fda.gov/medwatch/report.htm
Regular Mail: Use postage-paid FDA form 3500 available at:
www.fda.gov/MedWatch/getforms.htm.
Mail to MedWatch 5600 Fishers Lane, Rockville, MD 20852-9787
Fax: 1-800-FDA-0178

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Nestlé Withdraws Nestlé Farinha Lactea Cereal in the United States

Nestlé is withdrawing Nestlé Farinha Lactea cereal in the United States. Nestlé is taking this action as we have learned that the product may contain residual traces of a pesticide not currently approved for use on wheat in the U.S. While the pesticide is approved for use in Brazil and the noted levels are well below Brazilian standards, it is not used on wheat products in the United States and therefore there is no set standard for its presence in cereal. The pesticide is permitted in the United States on grain crops other than wheat.

Nestlé Farinha Lactea cereal is manufactured in Brazil by Nestlé Brazil and sold primarily in Portuguese language communities in the United States. The withdrawal applies to all sizes, varieties and production codes of the product. No other Nestlé products are affected.

Nestlé USA is assisting with the withdrawal of this product from the U.S. market to ensure the continued quality and safety of Nestlé products. Nestlé has not received any illness reports or consumer complaints.

Consumers who have purchased Nestlé Farinha Lactea cereal should not consume the product, and should return it to the store where they purchased it for a full refund.

We encourage consumers with questions about the withdrawal to contact Nestlé Consumer Services at (800) 628-7679.

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Everlasting Distributors Inc. Issues a Nationwide Recall of Fresh and Crispy Jacobina Biscuits Because of Possible Health Risks

TT Note: Oops- here comes another one.

Everlasting Distributors Inc., Bayonne NJ is initiating a nationwide recall of all their 3.88oz (110gm) packages of Fresh and Crispy Jacobina Biscuits because it may be contaminated with Melamine.

Consumers who have the product which is being recalled should stop using it immediately. If consumers have questions about possible health risks, they should contact their doctor.

Product was distributed nationwide in Asian Grocery stores.

The product comes in 3.88oz (110 gm) blue and red color clear plastic package, labeled “JACOBINA”.

No illnesses associated with this product have been reported to date.

The recall was initiated after FDA testing discovered that product was found to contain Melamine. Consumers who have purchased Fresh and Crispy Jacobina Biscuits are urged to return it to the place of purchase for a full refund. Consumers with questions may contact the company at 201-823-0800, Monday to Friday 9:00 to 5:00, Eastern Standard Time.

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Consumers Becoming Increasingly Less Tolerant of Recalls, Demanding More Control Over Information

TT Note: There are so many recalls in our markets. Have you ever stopped to see the country who appears to be the major manufacturer of the suspect items? Take a moment and go to the Fayette Front Page "Recall Roundup." We bring you all the recalls we can find on a daily basis. Be an informed consumer!

PRNewswire/ -- The buying habits of consumers change dramatically and cost companies millions when product safety and quality issues arise, according to a new study released today by Deloitte.

More than half of consumers responding (58 percent) who heard about product safety and/or quality problems changed their buying habits, according to the survey. These consumers turned away from such products for more than nine months, on average, increasing the likelihood that they would discontinue the use of the product or brand entirely.

"Our research shows that consumers are becoming less tolerant of recalls with more than 50 percent changing their product choices," said Pat Conroy, Deloitte LLP's vice chairman and consumer products practice leader. "As these consumers continue to buy different products, product manufacturers can expect lower sales and run the risk of damage to their brands."

The survey, "Food and Product Safety and Its Effect on Consumer Buying Habits," addresses consumer behavior around product safety and product quality issues in general. Specifically, it focuses on key issues in four product categories:

-- Toys
-- Consumer electronics
-- Fresh food
-- Packaged food/beverages


Of these categories, changes in buying habits were most common for fresh food and packaged food/beverage. Roughly half (49 percent) of respondents said they were extremely concerned about product safety, with the greatest concerns coming from women (53 percent) and consumers 55 years of age and older (56 percent). All in all, there is a wide awareness about product safety and quality problems, and more than half of respondents (54 percent) said they were more concerned about the safety of fresh food products than they were a year ago.

Global Concerns

The global lines that were once drawn have now begun to blur and corporate globalization has created "businesses without borders." However, though globalization is an increasingly valuable part of doing business, roughly two-thirds of consumers surveyed (65 percent) were extremely concerned about the safety of products produced outside the United States, with the greatest apprehension coming from older consumers.

Approximately three-quarters of the overall respondents (73 percent) were extremely concerned about the safety of products produced in China, with half having the same doubts about products produced in Southeast Asia and Mexico.

As products fall under greater scrutiny, consumers surveyed indicated they would like more information about the safety of food products provided on packaging (86 percent), company Websites (81 percent) and by the government (81 percent). Some 67 percent said that food product labels with country of origin labeling, certification of product testing and certification of quality testing would be extremely important in their buying decisions.

"Consumers' increased sensitivity of product safety and quality is having a long-term effect on business," said Conroy. "Product recalls impact companies' revenues and share price, as well as market share and brand perception. We've seen that, while some companies can maneuver through recalls relatively unscathed, others suffer catastrophic damage."

The research shows that some of the key factors that drive the extent of a product recall impact ranges from the extent of the company's product diversification, if the recall is specifically for a branded product, strength of the company's brand when the incident occurred and how the company responds.

"Companies are meeting consumers' concerns by upgrading or expanding safety procedures including stricter safety standards, testing and third-party audits and government intervention is driving change," said Conroy. "The recent granting of the Consumer Product Safety Commission to initiate product recalls and monitor ingredient levels such as lead allowed in toys and other children's products, is a very timely and relevant example of changes being made all with consumer safety and peace-of-mind at the top of the agenda."

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Statement Released by Mars Petcare US Regarding the Voluntary Recall of a Limited Number of Bags of Wal-Mart SPECIAL KITTY(R) Gourmet Blend Cat Food

PRNewswire-USNewswire/ -- Even though there is no link between the SPECIAL KITTY(R) Gourmet Blend dry cat food manufactured at the Allentown, Pennsylvania factory and any human or pet illness, we are taking precautionary action to protect pets and their owners by announcing a voluntary recall of all sizes of SPECIAL KITTY(R) Gourmet Blend produced at the facility on August 11, 2008. This action is being taken as a result of potential Salmonella contamination.

This voluntary recall affects only a limited number of bags of SPECIAL KITTY(R) Gourmet Blend dry cat food sold at Wal-Mart locations in Connecticut, Delaware, Massachusetts, Maryland, Maine, North Carolina, New Hampshire, New Jersey, New York, Ohio, Pennsylvania, Rhode Island, Virginia, Vermont, and West Virginia.

Mars Petcare has been working cooperatively with Wal-Mart to address this issue, and the affected product of this lot has already been removed from Wal-Mart's shelves. As a result, consumers can be assured that all SPECIAL KITTY(R) Gourmet Blend products that remain on Wal-Mart's shelves are safe and not subject to this recall.

Our top priority has always been and continues to be the health and welfare of pets and their owners, and we are working vigorously to identify the cause of the issue.

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FDA Detects Melamine Contamination in Flavored Drink

TT Note: And they just keep on coming-----

The U.S. Food and Drug Administration (FDA) has increased inspections and product testing efforts in response to the melamine contamination problem which originated in Chinese dairy products. As a result of the FDA’s on-going testing program, the agency has detected melamine contamination in Blue Cat Flavor Drinks. The distributor of the product, Tristar Food Wholesale Co. Inc., initiated a recall of several flavors of Blue Cat Flavor Drink, based on the FDA’s findings. The FDA advises the public not to consume this product and recommends that retailers and food service operators remove the product from sale or service.
Other Recalls

On September 26, the FDA issued an alert to consumers that seven Mr. Brown instant coffee and milk tea products were being recalled by the Taiwanese company, King Car Food Industrial Co. Ltd., due to possible contamination with melamine. King Car Food Industrial Co. used a non-dairy creamer manufactured by Shandong Duqing Inc., China, which was found to be contaminated with melamine. The recalled products are:

* Mr. Brown Mandheling Blend Instant Coffee (3-in-1)
* Mr. Brown Arabica Instant Coffee (3-in-1)
* Mr. Brown Blue Mountain Blend Instant Coffee (3-in-1)
* Mr. Brown Caramel Macchiato Instant Coffee (3-in-1)
* Mr. Brown French Vanilla Instant Coffee (3-in-1)
* Mr. Brown Mandhling Blend instant Coffee (2-in-1)
* Mr. Brown Milk Tea (3-in-1)

The FDA recommends that consumers not consume any of the above Mr. Brown instant coffee and milk tea products. The FDA also recommends that retailers and foodservice operators remove the products from sale or service.

Sunny Maid Corp. Monterey Park, Calif., who is an importer and distributor of Mr. Brown Instant Coffee products, is recalling the products in the United States.

The FDA is working with regulatory agencies in the United States as well as with other countries. The California Department of Public Health and the New Zealand Food Safety Authority reported that its testing of White Rabbit Creamy Candies has shown melamine contamination at high levels. In light of the widespread contamination of milk and milk-based products in China and the New Zealand Food Safety Authority’s finding, the FDA continues to recommend that consumers not eat White Rabbit Creamy Candy and that retailers and foodservice operations remove the product from sale or service.

A recall by QFCO Inc., Burlingame, Calif., of the White Rabbit Creamy Candies, is underway in the United States.

The FDA is closely monitoring these recalls and will continue to perform follow up activities of other recalls that may develop.

To date, the FDA is not aware of any illnesses in the United States stemming from consumption of Blue Cat Flavor Drinks, White Rabbit Creamy Candy, or the Mr. Brown instant coffee and milk tea products.

Individuals who have experienced any health problems after consuming Blue Cat Flavor Drinks, White Rabbit Creamy Candy, or any of the identified Mr. Brown coffee and tea products are advised to contact their health care professional.
Background

On September 12, 2008, in light of reports from China of melamine contaminated infant formula, the FDA issued a Health Information Advisory to assure the American public that there is no known threat of contamination in infant formula manufactured by companies that have met the requirements to sell such products in the United States. That advisory also warned members of Chinese communities in the United States that infant formula manufactured in China, possibly available for purchase at Asian markets, could pose a risk to infants.

The FDA had contacted the companies who manufacture infant formula for distribution in the United States and received, from the companies, information that they are not importing formula or sourcing milk-based materials from China.

At the same time, the FDA—in conjunction with state and local officials—began a nation-wide investigation to check Asian markets for Chinese manufactured infant formula that may have been brought into the United States. In particular, this effort focused on areas of the country with large Chinese communities, such as Los Angeles, San Francisco, Seattle and New York. To date, investigators have visited more than 1,800 retail markets and have not found Chinese infant formula present on shelves in these markets.

The FDA also advises consumers not to purchase infant formula manufactured in China from Internet sites or from other sources.

The FDA has taken, and will continue to take, proactive measures to help ensure the safety of the American food supply. In conjunction with state and local officials, the FDA will continue to visit Asian markets for food items that are imported from China and that could contain a significant amount of milk or milk proteins. In addition, the FDA has broadened its domestic and import sampling and testing of milk-derived ingredients and finished food products containing milk, such as candies, desserts, and beverages that could contain these ingredients from Chinese sources. Milk-derived ingredients include whole milk powder, non-fat milk powder, whey powder, lactose powder, and casein.

In addition to state and local governments, the FDA is working in close cooperation with Customs and Border Protection within the U.S. Department of Homeland Security, the U.S. Department of Agriculture, Centers for Disease Control and Prevention, other federal agencies, and foreign governments.

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FDA Updates Health Information Advisory on Melamine Contamination

TT Note: What next?

The U.S. Food and Drug Administration (FDA) is alerting consumers that seven Mr. Brown instant coffee and milk tea products manufactured in China are being recalled by the King Car Food Industrial Co. Ltd. due to possible contamination with melamine. The products, manufactured by China’s Shandong Duqing Inc., are:

* Mr. Brown Mandheling Blend Instant Coffee (3-in-1)
* Mr. Brown Arabica Instant Coffee (3-in-1)
* Mr. Brown Blue Mountain Blend Instant Coffee (3-in-1)
* Mr. Brown Caramel Macchiato Instant Coffee (3-in-1)
* Mr. Brown French Vanilla Instant Coffee (3-in-1)
* Mr. Brown Mandhling Blend instant Coffee (2-in-1)
* Mr. Brown Milk Tea (3-in-1)

The FDA recommends that consumers not consume any of the above Mr. Brown instant coffee and milk tea products. The FDA also recommends that retailers and foodservice operators remove the products from sale or service.

As of September 25, 2008, the FDA testing of milk based products imported into the United States from China has not found melamine contamination.

The FDA is working with regulatory agencies in other countries. The New Zealand Food Safety Authority reports that its testing of White Rabbit Creamy Candies has shown melamine contamination at high levels. In light of the widespread contamination of milk and milk-based products in China and the New Zealand Food Safety Authority’s finding, the FDA recommends that consumers not eat White Rabbit Creamy Candy and that retailers and foodservice operations remove the product from sale or service.

To date, the FDA is not aware of any illnesses in the United States stemming from consumption of either White Rabbit Creamy Candy or the Mr. Brown instant coffee and milk tea products.

Individuals who have experienced any health problems after consuming either White Rabbit Creamy Candy or any of the identified Mr. Brown coffee and tea products are advised to contact their health care professional.

Background

On September 12, 2008, in light of reports from China of melamine contaminated infant formula, the FDA issued a Health Information Advisory to assure the American public that there is no known threat of contamination in infant formula manufactured by companies that have met the requirements to sell such products in the United States. That advisory also warned members of Chinese communities in the United States that infant formula manufactured in China, possibly available for purchase at Asian markets, could pose a risk to infants.

The FDA had contacted the companies who manufacture infant formula for distribution in the United States and received, from the companies, information that they are not importing formula or sourcing milk-based materials from China.

At the same time, the FDA—in conjunction with state and local officials—began a nation-wide investigation to check Asian markets for Chinese manufactured infant formula that may have been brought into the United States. In particular, this effort focused on areas of the country with large Chinese communities, such as Los Angeles, San Francisco, Seattle and New York. To date, investigators have visited more than 1,400 retail markets and have not found Chinese infant formula present on shelves in these markets.

The FDA also advises consumers not to purchase infant formula manufactured in China from Internet sites or from other sources.

The FDA has taken, and will continue to take, proactive measures to help ensure the safety of the American food supply. In conjunction with state and local officials, the FDA will continue to check Asian markets for food items that are imported from China and that could contain a significant amount of milk or milk proteins. In addition, the FDA has broadened its domestic and import sampling and testing of milk-derived ingredients and finished food products containing milk, such as candies, desserts, and beverages that could contain these ingredients from Chinese sources. Milk-derived ingredients include whole milk powder, non-fat milk powder, whey powder, lactose powder, and casein.

In addition to state and local governments, the FDA is working in close cooperation with Customs and Border Protection within the U.S. Department of Homeland Security, the U.S. Department of Agriculture, other federal agencies, and foreign governments.

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Coming Soon: Generic Drugs from China

TT Note: Say it ain't so. Yet again, China appears to be on the brink of exporting more into the country and this time, it's something that could really hurt or kill us. With all the safety issues with all of the recalls, do you want to trust they will make drugs safe? Here's the full story from Consumer Affairs.

If you liked the heparin, dog food, lead-painted toys, toothpaste and truck tires from China, you'll be happy to hear that Chinese-made generic drugs are making their way to the U.S. While the development raises some safety concerns....

Read the story.

California packer makes largest U.S. beef recall

WASHINGTON (Reuters) - A California meatpacker accused of animal cruelty is making the largest U.S. meat recall on record -- 143 million lbs, the Agriculture Department said on Sunday

http://news.yahoo.com/s/nm/20080217/ts_nm/food_recall_hallmark_dc

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China, lead and coal mines

I've talked toxic about this before... the number of products coming from China laden with lead. Seeing all of the recalls for products I'm well aware of how many recalls include the manufacturing location of China. It's not just lead paint, it's also defective or below standard products.

In my toxic note on the subject I tossed out the possibility that they were out to get us... Who needs nuclear weapons when you can poison the kids and destroy the economy? Destroy the economy you say??? It's killing some of these companies to have to recall all the toys and other products.

Today a news story floated across my screen (posted below) that stated China had the worst record in the world for deaths in coal mines. I had thought all the lead based paints on toys and products from China might be happening due to the low cost of paint (maybe they bought all our rejects) or, as said earlier, a desire to cripple the U.S.

Now I'm thinking this through a little deeper. I know they have a large population in China. Maybe human life doesn't have a high enough value in China (by my standards).

All those people who are involved in painting our lead covered toys are being exposed on a much higher level than our kids. Expendable? Lower caste? Lead soaked brains make happy drones?

If they didn't make so many of our products it would be easier to boycott China-made. But that begs a bigger question. If we're not buying then where do the factory workers in China go? If life is bad for them now, and it must be horrific if they're breathing and touching lead all day, then what would it be like on the streets?

I think we need to toughen up our standards and figure out a way to enforce them. Big money involved in enforcement.

See how easy it is to get off on a tangent? I start writing about life and end up on enforcing regulations.

It would be interesting to do some comparative stats between life in America vs. life in China. Quality, life expectancy and other comparisons could tell an interesting story. Maybe I'll add that to my list of things to do someday.

Here's the story:

China's coal mines kill 3,786 in 2007
BEIJING - Accidents in China's notoriously dangerous coal mines killed nearly 3,800 people last year, state media reported Saturday — a toll that is a marked improvement from previous years, but still leaves China's mines the world's deadliest.

http://news.yahoo.com/s/ap/20080112/ap_on_re_as/china_deadly_mines