Wednesday, February 10, 2010
FDA Unveils Initiative to Reduce Unnecessary Radiation Exposure from Medical Imaging
CT, nuclear medicine, and fluoroscopic imaging have led to early diagnosis of disease, improved treatment planning, and image-guided therapies that help save lives every day. The FDA continues to support a strong dialogue between patients and physicians over the medical necessity and risk associated with these types of imaging studies.
However, like all medical procedures, CT, nuclear medicine, and fluoroscopy pose risks. These types of imaging exams expose patients to ionizing radiation, a type of radiation that can increase a person’s lifetime cancer risk. Accidental exposure to very high amounts of radiation also can cause injuries, such as skin burns, hair loss and cataracts. Health care decisions made by patients and their physicians should include discussions of the medical need and associated risks for each procedure.
“The amount of radiation Americans are exposed to from medical imaging has dramatically increased over the past 20 years,” said Jeffrey Shuren, M.D., J.D., director of the FDA’s Center for Devices and Radiological Health. “The goal of FDA’s initiative is to support the benefits associated with medical imaging while minimizing the risks.”
While there is some disagreement over the extent of the cancer risk associated with exposure to radiation from medical imaging, there is broad agreement that steps can and should be taken to reduce unnecessary radiation exposure.
For example, the radiation dose associated with a CT abdomen scan is the same as the dose from approximately 400 chest X-rays. In comparison, a dental X-ray calls for approximately one-half the radiation dose of a chest X-ray. Both diagnostics serve important, sometimes critical, public health needs.
Through the FDA’s regulatory oversight of medical imaging devices, such as CT scanners, and through collaboration with other federal agencies and health care professional groups, the FDA is advocating the adoption of two principles of radiation protection: appropriate justification of the radiation procedure and optimization of the radiation dose used during each procedure.
“Working together,” said Shuren, “the FDA and other organizations hope to help patients get the right imaging exam, at the right time, with the right radiation dose.”
The three-pronged initiative the FDA is announcing will promote the safe use of medical imaging devices, support informed clinical decision-making, and increase patient awareness of their own exposure.
The FDA intends to issue targeted requirements for manufacturers of CT and fluoroscopic devices to incorporate important safeguards into the design of their machines to develop safer technologies and to provide appropriate training to support safe use by practitioners. The agency intends to hold a public meeting on March 30-31, 2010, to solicit input on what requirements to establish.
Examples could include a requirement that these devices display, record, and report equipment settings and radiation dose, an alert for users when the dose exceeds a diagnostic reference level (the optimal dose for most patients), training for users, and a requirement that devices be able to capture and transmit radiation dose information to a patient’s electronic medical record and to national dose registries.
In addition, the FDA and the Centers for Medicare and Medicaid Services are collaborating to incorporate key quality assurance practices into the mandatory accreditation and conditions of participation survey processes for imaging facilities and hospitals. These quality assurance practices will improve the quality of oversight and promote the safe use of advanced imaging technologies in those facilities.
The FDA recommends that health care professional organizations continue to develop, in collaboration with the agency, diagnostic radiation reference levels for medical imaging procedures, and increase efforts to develop one or more national registries for radiation doses.
A dose registry would pool data from many imaging facilities nationwide, capturing dose information from a variety of imaging studies. This registry will help define diagnostic reference levels where they do not yet exist, validate levels that do exist, and provide benchmarks for health care facilities to use in individual imaging studies.
In a bid to empower patients and increase awareness, the FDA is collaborating with other organizations to develop and disseminate a patient medical imaging history card. This tool, which will be available on the FDA’s Web site, will allow patients to track their own medical imaging history and share it with their physicians, especially when it may not be included in their medical records.
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Thursday, March 12, 2009
Trying Times for Local Newspapers Across America
My dad's first job as a young teen was standing outside a huge theatre in a large city shouting those words and selling the paper. He remembered those days fondly as it was really cool to see the large acts like Lawrence Welk and the Big Bands come through town.
Gone are the days of young boys on their bicycles delivering newspapers throughout the neighborhoods. Do our youth of today even know they existed?
It is sad to see so many newspapers go down. The economy has certainly played its role in adding nails to the coffin. But I wonder how many editors contributed to their own demise by focusing on extreme sensationalism or negative news? Just a thought.
As Cities Go From Two Papers to One, Talk of Zero
By Richard PÉREZ-PEÑA
Published: March 11, 2009
The history of The Seattle Post-Intelligencer stretches back more than two decades before Washington became a state, but after 146 years of publishing, the paper is expected to print its last issue next week, perhaps surviving only in a much smaller online version.
And it is not alone.....http://www.nytimes.com/2009/03/12/business/media/12papers.html?_r=2&pagewanted=1&hp
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Friday, November 21, 2008
Is your Christmas Tree making You Ill
24-7-- Could it be your Christmas tree that's making you sick? Recent studies tend to support that theory. It seems that Christmas trees, either real or artificial can be a source of mold or allergens that can be the cause of those "sniffles" you seem to have at this time of the year.
In a recent study, mold spores in an apartment had a normal range of 500-700 spores per cubic meter. When the Christmas tree was added, the spores measured about 800 spores per cubic meter of air for the first three days. By day 14 the spores count had increased to 5,000 spores per cubic meter. If you have asthma or are prone to sinus infections you are likely to have a problem. The longer you leave the tree up the worse the contamination.
An artificial tree, stored in the attic or basement for a year can pose many of the same problems. It can acquire pollens, dust or mold. Taking the tree outdoors and washing it down can help. But that isn't always possible due to cold temperatures of the season.
Minnesota based WorldWide Oxide markets and EPA approved GREEN mold preventer Vital Oxide. Vital Oxide is totally safe, is odorless, and contains no harmful VOC's states company spokesman Tom Heller. Simply spray Vital Oxide onto the tree every few days during the season, and the mold or allergen problem will not be a factor in your home states Heller. Because Vital Oxide is odorless, you will not have to worry about some cover-up scent destroying your Christmas ambiance.
For more information on the studies visit the WorldWide Oxide web site at http://www.worldwideoxide.com.
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Friday, October 31, 2008
Everlasting Distributors Inc. Issues a Nationwide Recall of Fresh and Crispy Jacobina Biscuits Because of Possible Health Risks
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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Friday, October 24, 2008
CPSC and Carter's Advise Parents of Rashes Associated with Heat Transferred, or "Tag-less," Labels
This advisory applies to Carter's Fall 2007 product line. The Fall 2007 line utilizes a label on the inside back of the garment that has a raised surface with a solid, rather than a stenciled, background. This advisory does not apply to previous and current product lines, which utilize labels with stenciled backgrounds.
The garments, which were made in various countries, were sold at Carter's own retail stores and at department and national chain stores.
If your child develops a rash on the upper back after wearing garments that have a "tag-less" label with a solid background, you should stop using these garments. If the rash persists or worsens, you should contact your pediatrician. For additional information, visit Carter's website at http://www.carters.com/corporate/tagless_message.aspx, contact Carter's toll free at 1-888-282-4674 or by email at contactus@carters.com
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Wednesday, October 01, 2008
FDA Awards $5.2 Million in Grants to Further Food and Feed Safety
"These cooperative agreements support and enhance local food protection efforts consistent with our Food Protection Plan," said Michael Chappell, the FDA's acting associate commissioner for regulatory affairs. "The grants represent an important step in the FDA’s continued efforts to integrate and improve the effectiveness of food safety systems at the federal, state and local levels."
Prevention: Ruminant Feed Ban Support Program
The cooperative agreements for the Ruminant Feed Ban Support Program further enhance the infrastructure of state, territorial, and tribal animal feed safety and bovine spongiform encephalopathy (BSE) prevention programs. Under these cooperative agreements, state, territory, and tribal governments will enhance their feed/BSE safety programs to increase the ability to locate and visit companies involved in the manufacture, distribution, and transportation of animal feed as well as operations feeding ruminant animals, and to verify their compliance with the BSE/ruminant feed ban. Funds may also be used to conduct educational outreach activities and to develop materials needed to further enhance the industries' knowledge of and compliance with the BSE/ruminant feed ban. The awards were up to $250,000 and the states receiving them were Iowa, Mississippi, North Carolina and Washington.
Intervention: Food Safety and Security Monitoring
The grants for Food Safety and Security Monitoring provide funding to Food Emergency Response Network chemistry laboratories, laboratories essential to intervention efforts. The grants may be used for facility upgrades, training in current food testing methodologies, and increased laboratory sample analysis capacity, among other activities. In the event of a large-scale chemical terrorism event affecting food or food products, the recipient may be required to perform selected chemical analyses of food samples collected by the FDA or provided by other government agencies through the FDA. The states receiving these grants were Colorado, California and Ohio and were given up to $350,000.
Intervention: Innovative Food Defense
The Innovative Food Defense grants will generate novel solutions and outreach to address gaps in, or provide enhancement to, food defense nationwide -- for example, implementing the food defense programs in food establishments called the Assure, Look, Employees, Reports, and Threat or ALERT, and Employees Follow, Inspect, Recognize, Secure, and Tell or FIRST. Each recipient was awarded up to $40,000. The funded counties were Riverside County Dept. of Environmental Health (California) and Multnomah County Department of Health (Ore.). The funded states were Pennsylvania and South Carolina.
Response: Rapid Response Teams
The first-ever Rapid Response Team (RRT) cooperative agreement will develop, implement, exercise and integrate an all-hazards food and food-borne illness response capability to more rapidly react to potential threats to our food supply. The RRT, which is designed to operate in conjunction with other food and feed agencies within state programs, other state RRTs, FDA district offices, and state emergency operations centers, is another tool to enhance response capabilities.
The RRTs will respond to all food hazard incidents in the farm-to-table continuum of food production and delivery by using incident command structure response protocols, a formalized crisis management system. Each recipient was awarded up to $500,000 to exercise its response team, conduct a program assessment, purchase additional equipment and supplies, fund personnel, train, and share information and data as appropriate. The funded states were North Carolina, Massachusetts, California, Michigan, Florida and Minnesota.
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Friday, September 26, 2008
FDA Updates Health Information Advisory on Melamine Contamination
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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Hopkins Experts: Call for Warning Labels on Energy Drinks about Caffeine
Johns Hopkins scientists who have spent decades researching the effects of caffeine report that a slew of caffeinated energy drinks now on the market should carry prominent labels that note caffeine doses and warn of potential health risks for consumers.
"The caffeine content of energy drinks varies over a 10-fold range, with some containing the equivalent of 14 cans of Coca-Cola, yet the caffeine amounts are often unlabeled and few include warnings about the potential health risks of caffeine intoxication," says Roland Griffiths, Ph.D., one of the authors of the article that appears in the journal Drug and Alcohol Dependence this month.
The market for these drinks stands at an estimated $5.4 billion in the United States and is expanding at a rate of 55 percent annually. Advertising campaigns, which principally target teens and young adults, promote the performance-enhancing and stimulant effects of energy drinks and appear to glorify drug use.
Without adequate, prominent labeling; consumers most likely won't realize whether they are getting a little or a lot of caffeine. "It's like drinking a serving of an alcoholic beverage and not knowing if its beer or scotch," says Griffiths.
Caffeine intoxication, a recognized clinical syndrome included in the Diagnostic and Statistical Manual of Mental Disorders and the World Health Organization's International Classification of Diseases, is marked by nervousness, anxiety, restlessness, insomnia, gastrointestinal upset, tremors, rapid heartbeats (tachycardia), psychomotor agitation (restlessness and pacing) and in rare cases, death.
Reports to U.S. poison control centers of caffeine abuse showed bad reactions to the energy drinks. In a 2007 survey of 496 college students, 51 percent reported consuming at least one energy drink during the last month. Of these energy drink users, 29 percent reported "weekly jolt and crash episodes," and 19 percent reported heart palpitations from drinking energy drinks. This same survey revealed that 27 percent of the students surveyed said they mixed energy drinks and alcohol at least once in the past month. "Alcohol adds another level of danger," says Griffiths, "because caffeine in high doses can give users a false sense of alertness that provides incentive to drive a car or in other ways put themselves in danger."
A regular 12-ounce cola drink has about 35 milligrams of caffeine, and a 6-ounce cup of brewed coffee has 80 to 150 milligrams of caffeine. Because many energy drinks are marketed as "dietary supplements," the limit that the Food and Drug Administration requires on the caffeine content of soft drinks (71 milligrams per 12-ounce can) does not apply. The caffeine content of energy drinks varies from 50 to more than 500 milligrams.
"It's notable that over-the-counter caffeine-containing products require warning labels, yet energy drinks do not," says Chad Reissig, Ph.D., one of the study's authors.
Griffiths notes that most of the drinks advertise their products as performance enhancers and stimulants - a marketing strategy that may put young people at risk for abusing even stronger stimulants such as the prescription drugs amphetamine and methylphenidate (Ritalin). A 2008 study of 1,253 college students found that energy drink consumption significantly predicted subsequent non-medical prescription stimulant use, raising the concern that energy drinks might serve as "gateway" products to more serious drugs of abuse. Potentially feeding that "transition" market, Griffiths says, are other energy drinks with alluring names such as the powdered energy drink additive "Blow" (which is sold in "vials" and resembles cocaine powder) and the "Cocaine" energy drink. Both of these products use the language of the illegal drug trade.
Griffiths and colleagues are currently collecting case reports of intoxication from energy drinks in children and adolescents. If readers are interested in learning more, go to http://www.bpru.org/energydrinks/ .
Eric C Strain, M.D., from Johns Hopkins also contributed to this study.
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Monday, September 22, 2008
Compromised US and Chinese Computers Launch Greatest Number of Cyber Attacks, According to SecureWorks' Data
This was followed by Brazil with over 166,987 attempted attacks, South Korea with 162,289, Poland with 153,205, Japan with 142,346, Russia with 130,572, Taiwan with 124,997, Germany with 110,493, and Canada with 107,483.
"We believe these statistics are significant because it clearly shows that the United States and China have a lot of vulnerable computers that have been compromised and are being used as bots to launch cyber attacks," said Hunter King, security researcher for SecureWorks. "This should be a warning to organizations and personal computer users that, not only are they putting their computers and networks at risk by not securing them, but they are actually providing these cyber criminals with a platform from which to compromise other computers."
Computer security can be greatly improved by keeping your web browser and operating system up to date, using the latest versions of antivirus and antispyware software, following safe computer practices such as being wary of the websites you visit, and not clicking on attachments and links within emails until verifying that the sender intentionally sent the enclosed link or attachment."
"These findings illustrate the ineffectiveness of simply blocking incoming communications from foreign IP addresses as a way to defend your organization from cyber attacks, as many hackers hijack computers outside their borders to attack their victims," said Don Jackson, Director of Threat Intelligence for SecureWorks. "The Georgia/Russia cyber conflict was a perfect example of this. Many of the Georgian IT staff members thought that by blocking Russian IP addresses they would be able to protect their networks, however, many of the Russian attacks were actually launched from IP addresses in Turkey and the United States so consequently they were hit hard. This was a perfect example where we saw Russian cyber criminals using compromised computers outside their borders."
"On the other hand, we have found that many of the Chinese hackers will compromise large networks within their own country and use them as bots to attack other organizations," continued Jackson. "For example, entire university networks in China will belong to local hacker groups."
"China's hackers do create botnets from spamming through email and blogs, but a relatively larger percentage of the compromised hosts under Chinese control are simply machines in schools, data centers, companies -- in other words, on large networks -- that are mostly unguarded and consequently are entirely controlled by hacker groups, as opposed to distributed bots harvested from widely distributed international spam runs, said Jackson. "And often the groups have an insider in the networks they own. We also see many local hacker groups in Japan and Poland compromise hosts within their own country to use in cyber attacks, so the Chinese hackers are not alone in using resources within their own borders."
With hackers utilizing computer resources inside and outside of their borders, SecureWorks suggests that in addition to securing computers with ongoing system and security updates and patches, organizations should utilize a black list to block inbound communications from known malicious IP addresses. Organizations should also block outbound communications to foreign countries known to harbor hackers and block outbound communications to hostile networks known to host criminal activity. This way if your organization does have an infected host within its network, then the host will be blocked from sending personal or company data to the cyber criminals. Of course, some of these hostile networks do support a handful of legitimate sites. In addition to a blacklist, your organization can use a separate whitelist to allow outbound communication only to trustworthy sites on those otherwise hostile networks.
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Thursday, September 18, 2008
FDA Proposes Label Requirements for Refused Imported Foods
"This system will make it more difficult for food importers to evade import controls after being denied admission into the United States," said Randall Lutter, Ph.D., deputy commissioner for policy. "It will complement our ongoing efforts to monitor food imports."
When FDA refuses to admit a food into the United States, the food must be exported or destroyed. But some persons attempt to bring the refused food back into the United States in the same condition by shipping it to another U.S. port in hopes that the food will be admitted there.
The proposed regulation would require that shipping containers of food barred from entry, and any accompanying documents, be labeled as refused. The label would make it easier for FDA to detect previously-refused food.
The proposed rule implements a provision of the Public Health Security and Bioterrorism Preparedness and Response Act of 2002, which provided the FDA with new authority to protect the nation’s food supply.
Under the proposed rule, all owners or consignees of refused food would be required to affix a label to the shipping container that reads: "UNITED STATES: REFUSED ENTRY" in clear, conspicuous, print. A label would also have to be affixed to all documents accompanying the imported food such as invoices, bills of lading, and electronic documents.
The FDA will accept comment on the proposed regulation for 75 days following its publication in the Federal Register. Written comments may be submitted to:
http://www.regulations.gov/fdmspublic/component/main?main=DocketDetail&d=FDA-2007-N-0465
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Friday, September 12, 2008
Health Alert in Chinese Manufactured Infant Formula
In response to reports of contaminated milk-based infant formula manufactured in China, the U.S. Food and Drug Administration (FDA) today is issuing a Health Information Advisory. This is 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 infant formula in the United States. Although no Chinese manufacturers of infant formula have fulfilled the requirements to sell infant formula in the United States, FDA officials are investigating whether or not infant formula manufactured in China is being sold in specialty markets which serve the Asian community.
The FDA is advising caregivers not to feed infant formula manufactured in China to infants. This should be replaced with an appropriate infant formula manufactured in the United States as mentioned below. Individuals should contact their health care professional if they have questions regarding their infant’s health or if they note changes in their infant’s health status.
The FDA began investigating the reports of contamination immediately and received information from the companies who manufacture infant formula for the American market that they are not importing infant formula or source materials from China. The following manufacturers have met the necessary FDA requirements for marketing milk-based infant formulas in the United States: Abbott Nutritionals, Mead Johnson Nutritionals, Nestle USA, PBM Nutritionals, and Solus Products LLC. Also, one manufacturer, SHS/Nutricia, Liverpool, England, markets an amino acid based exempt infant formula that does not contain any milk-derived ingredients.
We are asking state officials to work with the Agency to assist with the removal of any Chinese infant formula found on store shelves, and to warn members of the Asian community to avoid using Chinese manufactured infant formula.
It has been reported that a number of infants in China who have consumed Chinese manufactured infant formula are suffering from kidney stones, a condition which is rare in infants. The Chinese manufactured infant formula may be contaminated with melamine. Melamine artificially increases the protein profile of milk and can causes kidney diseases such as those seen in these Chinese infants.
FDA requires that all infant formula manufacturers register with the Agency and adhere to specific labeling and nutritional requirements. All properly registered infant formula manufacturers marketing infant formula in the United States undergo an annual inspection of their production facilities.
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Wednesday, September 10, 2008
September 11th, 2008
A month of so after the attack, when everyone was still sporting American flags on their lapels and in their yards, I remember talking to my husband about the renewed patriotism and the single spirit we as a nation seemed to have at the time. I hated the reason, but was thrilled to see such a monumental change in our country's attitudes.
I thought he was being overly cynical when he said it wouldn't last very long. Unfortunately, he was right and I was wrong.
It didn't last very long in the scheme of things. It didn't take long for the flags to fade from the windshields and the solidarity t-shirts to end up in the rag bag.
If anything, we seen to be more divided than we were before 9/11. Politics is nastier than ever. Less seems to be done every day to promote our love of country.
Everyone supports the troops now, at least on the surface. Some of us truly care and believe, others mouth the sentiment because it is politically correct to do so. It's also a potential career killer if you don't talk the talk at least, even while doing damage to the cause for which they're fighting.
Tomorrow John McCain and Barack Obama will hold a truce for a short day, then go back to fighting.
Tomorrow school children will be fed a spoonful of information about September 11th. Then they will go back to their normal lessons and play.
Tomorrow people will dig out their flags and spend a few moments reflecting on the horrific day that changed our world. Then they'll pack up the flags and patriotism for the year and go back to their routine and forget about it all for another year.
I'm proud that we have some who value their freedoms and are willing to fight for them. I'm not simply talking about our soldiers who put their lives on the line to protect those freedoms. I'm talking about groups like the Sons and Daughters of the American Revolution who try to promote patriotism throughout the year. I'm talking about individuals who make sure their flags are flown properly and who make sure they always fly. I'm talking about those who work in so many ways to help protect the Constitution, the Declaration of Independence and all that has made our country shine.
We need our patriots, we need those who love our country and we need people who are able to look beyond their own needs to see the bigger picture.
We need to remember September 11 and it's lessons every day, not just one day a year.
- jmd
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Thursday, September 04, 2008
“Private Browsing” Not So Private
(BUSINESS WIRE) --Microsoft announced last week that the upcoming Internet Explorer 8 would include the rumored “private browsing” mode, designed to conceal a user’s activities from other users of the same PC. A privacy mode is already a feature of Apple’s Safari browser, and a similar technology is available in Mozilla’s Firefox, as well as the newly announced Google Chrome. Private browsing mode utilizes techniques that automatically delete search history, page cache, and browsing history so the next user can’t see where you’ve been or what you’ve been up to.
Unfortunately, this mode does nothing to provide real privacy from hackers, spyware, and network-based attacks that pose significant and growing threats to users’ finances and identities.
“The private browsing mode avoids embarrassment, and prevents your spouse from learning about the surprise gift you’re researching for them,” says Ray Dickenson, Authentium’s CTO. “But it doesn’t prevent the disclosure of your usernames, passwords, credit card numbers, and other personal information to criminals. While we applaud the feature as a valuable tool for users, we’re concerned the name will only exacerbate the current explosion of digitally cultivated identity theft by fooling users into thinking they’re protected.”
Authentium, maker of the leading secure browsing companion SafeCentral, cautions users not to trust these privacy features as a means of protection from fraud.
“Whether using Safari, Firefox, or the upcoming Internet Explorer 8, users need to be aware that the private browsing mode is for local protection only, and is not a deterrent against identity theft,” says Corey O’Donnell, Vice President of Marketing for Authentium. “While I can’t suggest a better name, we’re certainly concerned that the private browsing moniker will give users a false sense of security and put them at increased risk when conducting transactions online. Independent of our goals and mission of providing advanced protection with our SafeCentral service, we feel it’s important to alert the public about the actual functions of this feature.”
Authentium issued the warning in conjunction with the recent announcement and posted notifications to its antivirus customers and security partners via the corporate blog. Authentium is attempting to ensure that the security community, including its roster of high-profile partners, was prepared to respond to customer inquiry on the feature.
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Saturday, August 30, 2008
Nothing Toxic About Sarah Palin
The Dems are saying Palin was a contrived pick to get the women. To me that is demeaning. What they're basically saying is that any woman would have brought the women (aka pied piper rats?) to the voting booth. I have news for you guys, we are picky about who we support, man or woman.
Palin is the entire package. She has balanced family and job and still managed to look good doing it. She doesn't seem to ruffle easy, she's not intimidated by the good-old-boys and man is she sharp.
There is electricity in the air. McCain showed the Democrats what "change" is all about. It's not a guy who has spent his life re-writing himself and grooming himself to be the President. This is what real is all about. This is what change is all about.
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Friday, August 08, 2008
Watchdog and Russell Jones & Walker Provide Sofa Injury Claims Update
24-7 - Back in February, the BBC's Watchdog programme exposed a story about leather sofas, sold by a number of leading high street retailers, which had caused severe skin reactions in some people. The Chinese manufactured sofas, the majority of which were purchased from Land of Leather, Argos and Walmsleys, were thought to contain a chemical which was causing extreme allergic reactions in some people, including rashes and blistering that resulted in hospitalisation for some.
Watchdog reported on 12 May 2008 that, in conjunction with Russell Jones & Walker (RJW), it has since discovered that the cause of these 'sofa burns' is Di-methyl Fumarate (DMF), a chemical known to cause skin irritation. This fungicide is contained within a sachet which is placed inside the sofas in order to protect against mould during storage, transit and everyday usage. Argos' independent investigations have also now confirmed these results.
A team of Solicitors led by Richard Langton and Christian Shotton of RJW is currently representing [url=http://www.rjw.co.uk/"]injury claims[/url] on behalf of more than 500 people who have suffered due to the affected sofas, and this number is continuing to grow. Around 1000 individuals are now launching a group action in the high court to sue the retailers who sold the sofas for damages.
The majority of the sofas have now been recalled, but a list of known affected sofa batch numbers has been compiled on the RJW Solicitors site in order to enable worried consumers to check whether their sofa might be one of those affected.
In light of the ongoing problem, RJW Solicitors has also advised that anyone who has experienced similar skin problems, even if their sofa's batch number does not appear in the list, should still contact the retailer where they originally purchased the sofa from.
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Wednesday, August 06, 2008
Nine Firms Agree To Pay More Than $350,000 in Civil Penalties For Failing To Timely Report Drawstrings In Children's Outerwear
The firms paying the penalties are:
AJ Blue LLC, of New York City, N.Y.
A&R Knitwear Inc., of New York City, N.Y.
Cobmex Inc., of Lakewood, Calif.
Liberty Apparel Co. Inc., of New York City, N.Y.
Rebelette International Trading Corp., of South El Monte, Calif.
Scope Imports Inc., of Houston, Texas
Sears Holdings Management Corp., of Hoffman Estates, Ill.
Siegfried & Parzival Inc., of City of Industry, Calif.
Vacation Clothing Exchange Inc., d/b/a Basix USA, of Lauderdale Lakes, Fla.
In February 1996, CPSC issued drawstring guidelines (pdf) to help prevent children from strangling or getting entangled on the neck and waist drawstrings in upper outerwear, such as jackets and sweatshirts. In May 2006, CPSC's Office of Compliance announced (pdf) that children's upper outerwear with drawstrings at the hood or neck would be regarded as defective and a substantial risk of injury to young children.
Federal law requires manufacturers, distributors, and retailers to report to CPSC immediately (within 24 hours) after obtaining information reasonably supporting the conclusion that a product contains a defect which could create a substantial risk of injury to the public, presents an unreasonable risk of serious injury or death, or violates a federal safety standard.
In agreeing to settle the matters, the firms deny CPSC's allegations that they knowingly violated the law.
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Monday, August 04, 2008
Companies Agree To Cut Cancer-Causing Chemicals In Potato Chips
The state of California has settled lawsuits against Heinz, Frito-Lay, Kettle Foods and Lance Inc. after the companies agreed to slash levels of the cancer-causing chemical.....
Read the story.
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Wednesday, July 30, 2008
FDA Extends Consumer Warning on Serrano Peppers from Mexico
Laboratory testing by the U.S. Food and Drug Administration has confirmed that both a sample of serrano pepper and a sample of irrigation water collected by agency investigators on a farm in the state of Nuevo Leon, Mexico, contain Salmonella Saintpaul with the same genetic fingerprint as the strain of bacteria that is causing the current outbreak in the United States.
As a result, until further notice, the FDA is advising consumers to avoid raw serrano peppers from Mexico, in addition to raw jalapeño peppers from Mexico, and any foods that contain them.
The test results announced today are part of the FDA's continuing intensive investigation into the outbreak of Salmonella Saintpaul. The investigation has involved tracing back, through complex distribution channels, the origins of products associated with clusters of illness in the United States, as well as inspections and evaluation of farms and facilities in this country and in Mexico, and the collection and testing of environmental and product samples. One of these tracebacks led to a packing facility in Mexico, and to a particular farm, where the agency obtained the samples.
Previously, FDA inspectors collected a positive sample of jalapeño pepper from a produce-distribution center owned by Agricola Zaragosa in McAllen, Texas. The FDA continues to work on pinpointing where and how in the supply chain this first positive jalapeño pepper sample became contaminated. It originated from a different farm in Mexico than the positive samples of serrano pepper and irrigation water.
The FDA is still analyzing many of the samples taken at various farms in Mexico. If laboratory results warrant, the FDA will provide consumers with additional cautions or warnings necessary to protect their health.
On July 17, the FDA announced it had determined that fresh tomatoes now available in the domestic market are not associated with the current outbreak. As a result, the agency removed its June 7 warning against eating certain types of red raw tomatoes.
FBI Warns of Storm Worm Virus
A botnet is a collection of compromised computers under the remote command and control of a criminal “botherder.” Most owners of the compromised computers are unsuspecting victims. They have unintentionally allowed unauthorized access and use of their computers as a vehicle to facilitate other crimes, such as identity theft, denial of service attacks, phishing, click fraud, and the mass distribution of spam and spyware. Because of their widely distributed capabilities, botnets are a growing threat to national security, the national information infrastructure, and the economy.
“The spammers spreading this virus are preying on Internet users and making their computers an unwitting part of criminal botnet activity. We urge citizens to help prevent the spread of botnets by becoming web-savvy. Following some simple computer security practices will reduce the risk that their computers will be compromised,” said Special Agent Richard Kolko, Chief, FBI National Press Office.
Everyone should consider the following:
* Do not respond to unsolicited (spam) e-mail.
* Be skeptical of individuals representing themselves as officials soliciting personal information via e-mail.
* Do not click on links contained within an unsolicited e-mail.
* Be cautious of e-mail claiming to contain pictures in attached files, as the files may contain viruses. Only open attachments from known senders.
* Validate the legitimacy of the organization by directly accessing the organization's website rather than following an alleged link to the site.
* Do not provide personal or financial information to anyone who solicits information.
Tuesday, July 29, 2008
What's Lurking in Your Granite Countertop Can Kill You!
But then again, those of us who live anywhere near "radon central - big granite outcrop" most likely don't have to worry about a few extra linear feet in our homes. Gee, I wonder who wrote this story?? Must have been someone who is between a rock and a hard place.
24-7 - When marketing a product, one expects a bit of hype. The idea is to show that the product is the best over the competitor's line of product. That is the trade of advertisers and the history of marketing. Some tactics used to sell can be humorous or as serious as the competition between manufacturers. Marketing tactics that play on fears of the general public can be a very powerful tool.
In the present day, there's a very popular angle of "green." This is prevalent everywhere in the media. So what happens when you mix a scare tactic under the guise of environmental concern?
Buildclean found the answer to that question. The premise seems of the nonprofit organization seems to be admirable but the fact that the "awareness campaign" that Buildclean is currently using seems to be curiously slanted. In fact, the target seems to be the natural stone industry.
When Sara Selber of BuildClean was asked how she got involved in natural stone and radon, she explained how she was approached by the owner of C&C North America, a company that produces two products - granite and a quartz product called Silestone.
"C&C North America then recruited a quartz company called Cambria, after they learned quartz was an issue, she further explained that the two companies hired her to test quartz, granite and other surfaces for radon emission. Both companies are testing their products through BuildClean, and they contracted two labs - one in New York and one in Israel.
We have looked all over the C&C website but cannot find any mention of natural stone.
When ask what granites emit radon, Sara Selber said; "Not all granites emit radon or radiation. There are some that clearly do. There are some that absolutely don't. We don't know," she said.
They're being set up as a non-profit, and they're funded with two large donations.
The first is $250,000 from the makers of 'Silestone.' They manufacture quartz countertops, which is a direct competitor to granite. Silestone finance records show that they started out in April of 1998 with a an initial investment of $410K, made there first million in 1998, sales in 2002 was over $70M, and sales in 2006 was well over $260M. it is not hard to see that they have the money to invest $250,000 in a new advertising campaign.
BuildClean is also getting money from Cambria, another quartz manufacturer. In fact, Cambria's marketing director is on BuildClean's board of directors.
When asked about the funding Sara responds: I don't believe the issue is who our founders are. And I'm not going to have that debate." That answer seems to be clear enough.
In a recent interview Mrs. Selber mentions teaming up with Al Gerhart who has some interest in the granite radon scare.
Al Gerhart is a carpenter who happens to own a website called the Solid Surface Alliance .org. He educated himself, regarding materials he works with that may expose him to harmful elements.
Upon further review it seems this "personality" is well known for his view of natural stone. All one has to do is look at the website to get the gist of his viewpoint. Coincidentally, there also seems to be a new business venture for Solid Surface Alliance as the website now sells Geiger counters to detect radiation...
His debates have earned him quite a place online in forums discussing the subject.
After a certain debate on a well known residential forum, a renowned geoscientist in the industry concluded:
"Al attempts to hijack debates by choking the system with verbal diarrhea. The problem appears to be that he has a bit of knowledge about some things but not enough sense and understanding of the subjects. In that debate on the Garden Forum he threw in so many fabrications (plain made up lies) that his credibility just plummeted to zero.
Anyone who operates this way (by including a number of facts to gain an element of credibility in the eyes of a generally uninformed audience, twisting facts deliberately or because of his lack of understanding, and then throwing in a number of lies) does not deserve extended airtime. Many years ago when doing science psychology I still remember my professor giving the advice to his students that you should never engage a nutter in debate. You can never win an argument with such people. I recognized this early in the forum and that is why I would not engage him in "debate".
One of his major problems is that he does not know what the numbers mean and how they are derived."
In response to the BuildClean(TM) tactics, The Marble Institute of America is in the process of doing their own independent study:
"The Marble Institute of America (MIA) is grateful for the preliminary response from the members to the newly established Truth About Granite Fund. Based on this positive response, it's clear that their colleagues share their commitment to protect consumers from needless fear mongering by establishing standards for the testing of granite so consumers can safely and comfortably enjoy the beauty, durability and practicality of this natural stone."
When we asked the MIA why Sara Speer Selber consider The Truth About Granite Fund as a draconian move that is being waged against BuildClean(TM), they simple responded:
"The Truth About Granite Fund was established to help raise funds to develop unbiased, scientific standards for the granite industry, including the testing of granite for radon. No such standards currently exist in the natural stone industry. Previous tests of granite samples have found they are safe. However, the Truth in Granite Fund aims to take advantage of new, advanced scientific instruments that make testing both more practical and more accurate. Our goal is to make sure testing follows consistent protocols, so that future studies are meaningful and based on consistent, approved science - not isolated methodologies or unapproved instruments. Ultimately, our goal is to make sure the granite we sell is safe."
This latest sales tactic received the attention of an independent group called the Natural Stone Restoration Alliance (NSRA). The NSRA saw Radon testing as an added service that their members could provide to the homeowners along with all their other services for natural stone. Josveek Huligar, one of the lead testers and trainer for the NSRA , invited times Members of the Solid Surface Alliance dot org to discuss and provide proof of this threat to the home owners.
The Solid Surface Alliance dot org agreed to provide an alleged radiation producing granite sample that they claim to have in their possession to do independent testing. After an initial agreement between the two groups it seems the Solid Surface Alliance dot org has reneged on the delivery of the alleged material. Mr Huligar was disappointed of the outcome. The NSRA than requested the name of the company that Mr. Gerhart claimed to just have rejected over 10k worth of radon producing granite. When the information was not provided, Huligar ask if he could purchase the next slab that Mr. Gerhart rejected. But for some reason Mr. Gerhart could no longer find a sample for testing. Mr. Huligar went on to say: "All we care about at this point. As for whether are not Stone adds a measurable amount of "radon" in a home, Mr. Gerhart had agreed to come to NY and pick out a hot slab that I would place in my own home after testing my home for radon. Once the granite was installed I would test my home again as described by the EPA and have it tested by someone approved by the EPA. Not only would we do the short and long term test, we would also video tape the whole event, the selection, the creation, the install, and than setting up cameras for anyone to view the stone and meters on the net. I was looking forward to do this, but at this time it appears that Mr. Gerhart has no plans on doing as he said which is a big disappointment."
The NSRA plans to push for this simple test, they feel that the consumers only care about one thing; "whether or not adding granite in your home would significantly change the radon levels in a home". At present, the most prudent consumer should watch the outcome of this debate and make an informed decision, not taken in by a scare tactic by advertisers.
EPA Confirms That Granite Countertops Pose No Significant Health Risk. Click here to read their story.
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