Tuesday, August 2, 2011
The link follows: http://www.totalrecallinfo.com/freerecalls.php?id=25066
Please accept our apologies to all affected individuals.
The RAPEX rescind notice does not state the reason for this order.
Saturday, July 23, 2011
The Austrian RAPEX-contact-point would like to withdraw notification nr. 0812/10 Elbow Shock Absorber and asks you to remove the notification permanently from the RAPEX-System.
The reason is, that the Belgium authorities have classified this product as a medical device and the Austrian authority for medical devices does not think, that the notified problem has to be seen as a systematical failure of the product. The content of mercury is not seen as a problem.
The Austrian authorities, competent for general product safety, are still concerned about the high amount of mercury, but because of the classification as medical device, there is no further possibility to ban the product on the basis of the product safety act.
FEDERAL MINISTRY OF
LABOUR, SOCIAL AFFAIRS AND
Unit III/2 Product Safety
Austrian RAPEX-Contact Point
Stubenring 1, 1010 Vienna
Phone: +43 (1) 711 00 - 2513
Tuesday, July 19, 2011
Through the CPSIA, Congress set tough new levels for lead content in products designed or primarily intended for children 12 and younger. Lead is a heavy metal that is toxic for children, and associated with lowered levels of learning, impaired hearing, brain damage and, at high levels, can be fatal.
Congress directed CPSC to phase in the reduced levels for lead content over a three year period, starting with 600 ppm on February 10, 2009. The level dropped to 300 ppm on August 14, 2009. Finally, Congress directed the total lead content limit be set at 100 ppm, unless the Commission determined it was not technologically feasible for a product or product category.
The Commission was not able to determine that 100 ppm total lead content is not technologically feasible, as staff found that materials containing less than 100 ppm total lead content are commercially available in the marketplace for manufacturers. CPSC staff also found many products currently on the market, that have been tested by CPSC or other organizations, that are already in compliance with the new 100 ppm total lead content limit.
Starting on August 14, 2011, manufacturers, importers, retailers and distributors of children’s products must comply with the new 100 ppm federal limit for total lead content. CPSC will not enforce the CPSIA’s independent third party testing requirement for total lead content until December 31, 2011, due to a stay of enforcement that is already in place.
The stay of enforcement does not apply to children’s metal jewelry, which currently must undergo independent third party testing.
The new 100 ppm lead content limit does not apply to inaccessible (internal) parts of children’s products and certain component parts of children’s electronic devices, like electronic connectors and plugs, including headphone plugs.
Lead content levels for children’s products are different from the levels Congress set for lead in paint or surface coatings. The limit for lead in paint or surface coatings is .009 percent. The .009 percent level has been in place since August 14, 2009 and independent third party testing is required for all paints or surfaces coatings used on children’s products.
CPSC Hotline: (800) 638-2772
CPSC Media Contact: (301) 504-7908
Sunday, June 19, 2011
In less than two weeks, a new generation of safer cribs will be for sale in retail stores across the country. On June 28, 2011, anyone that manufactures or sells baby cribs will be required to meet new and improved crib safety standards approved by the U.S. Consumer Product Safety Commission on December 15, 2010.
Today, the Commission voted 4-0-1 to extend the length of time that short-term crib rental companies have to comply with the new mandatory standards for full-size and non-full-size baby cribs. This extension gives crib rental companies until December 28, 2012 to update their inventory with compliant cribs, which is the same deadline for the public accommodation facilities that these companies serve.
When the Commission approved the new rules in 2010, child care facilities, such as family child care homes and infant Head Start centers, and places of public accommodation, such as hotels and motels, were given until December 28, 2012 to have compliant cribs in their facilities.
Today’s vote by the Commission does not change the requirements on manufacturers or retailers of cribs. The Commission voted 3-2 today against granting an extension for retailers to comply with the new crib safety requirements. In turn, the Commission will continue to require companies that manufacture or sell cribs in the United States to comply with the new federal safety standards effective June 28, 2011.
Federal mandatory crib standards had not been updated in nearly 30 years and the new rule will usher in a safer generation of cribs. These mandatory standards will: 1) stop the manufacture and sale of dangerous, traditional drop-side cribs; 2) make mattress supports stronger; 3) improve slat strength, 4) make crib hardware more durable; and 5) make safety testing more rigorous.
The new safety standards aim to keep children safer in their cribs and prevent deaths resulting from detaching crib drop-sides and faulty or defective hardware.
These crib standards were mandated by the Consumer Product Safety Improvement Act of 2008 (CPSIA). For more information on crib safety and safe sleep environments for baby, visit CPSC’s crib information center at: www.cpsc.gov/cribs
CPSC Recall Hotline: (800) 638-2772
CPSC Media Contact: (301) 504-7908
Thursday, May 19, 2011
The FSMA, signed by President Barack Obama, gives the federal Food and Drug Administration sweeping new authority to inspect, regulate and if needed, shut down any company along the food chain that is involved in product recalls and incidents of food-borne illness. It grants the FDA power to act if it suspects a "reasonable probability" of an outbreak occurring, and virtually unlimited authority in case of an actual outbreak.
Under a "phased approach" similar to the way the United Kingdom implemented its food-inspection regime in 1990, the FSMA's first two rules will take hold this summer, Steven Thompson, senior adviser at London-based red24 security consultancy, said during A.M. Best Co.'s webinar, Food Safety: What Agents and Brokers Need to Know About New FDA Recall Authority. It was sponsored by Liberty Underwriters International and hosted by Best's Review magazine.
The first rule allows the FDA to detain food it believes has been produced under unsanitary or unsafe conditions for 30 days while regulators determine whether further action is required. The second rule requires anyone importing food into the United States to inform the FDA if any country has refused entry to the same product, including animal feed.
Tuesday, May 10, 2011
Consumer Inquiries: 888-INFO-FDA
Consumers warned to avoid eating oysters from area 1642 in Apalachicola Bay, Florida Warning follows bacterial illness outbreak
• The U.S. Food and Drug Administration is advising consumers, restaurant operators, commercial shippers and processors of shellfish not to eat, serve, purchase, sell or ship oysters from Area 1642 in Apalachicola Bay, Fla. because the oysters may be contaminated with toxigenic Vibrio cholerae serogroup O75.
• Nine persons have been reported with illness. For eight, the illness was confirmed as caused by toxigenic Vibrio cholerae O75; laboratory confirmation is pending in the other person. No one was hospitalized or died.
• All ill persons reported consumption of raw or lightly steamed oysters.
• Traceback indicates that oysters harvested from Area 1642 in Apalachicola Bay, Fla., between March 21 and April 6, 2011, are associated with illness.
• Those who have recently purchased oysters should check with the place of purchase and ask if they were harvested from the affected growing area.
What is the problem?
Raw oysters harvested from Area 1642 in Apalachicola Bay, Fla. between March 21 and April 6, 2011, have been linked to eight confirmed and one possible case of toxigenic Vibrio cholerae O75 infection. The ill persons ate raw or lightly cooked oysters harvested from that area. Ill persons reside in Florida, Georgia, Louisiana and Indiana; all report consumption of oysters while in Florida. There are several designated harvest areas within Apalachicola Bay, Fla, and each of these has a unique numerical identifier. Area 1642 is a zone that stretches from north to south in Apalachicola Bay just on the east side of the bridge that goes from Eastpoint, Fla., to St. George Island, Fla. The zone is approximately two miles wide from east to west.
What are the symptoms of Vibrio illness?
Illness is typically characterized by nausea, vomiting and diarrhea. The symptoms begin from a few hours up to five days after consumption of raw or undercooked seafood, particularly shellfish, or after ingestion of surface waters.
Who is at risk?
Persons at risk are those who traveled to Florida and consumed oysters that were harvested from Area 1642 of Apalachicola Bay or who purchased oysters in a state to which these oysters or oyster product were distributed and ate them.
What do consumers need to do?
Those who have recently purchased oysters should check with the place of purchase and ask if they were harvested from the affected growing area. If the oysters were definitely or possibly harvested from Area 1642 in Apalachicola Bay, Fla., and have not yet been consumed, they should not be eaten. If the oysters were already consumed and no one became ill, no action is needed. If you develop a diarrheal illness within a week after consuming raw or undercooked shellfish, see your healthcare provider and inform the provider about this exposure.
Those with weakened immune systems, including people affected by AIDS, chronic alcohol abuse, liver, stomach, or blood disorders, cancer, diabetes, or kidney disease should avoid eating raw oysters, regardless of where they are harvested.
What product forms are included in the recall?
This advisory, which comes from an outbreak of illness caused by toxigenic Vibrio cholerae O75, applies to live in-shell and shucked fresh or frozen oysters from the area.
Where is it distributed?
These oysters or oyster product were initially distributed in Florida, Alabama, Georgia, Mississippi, and North Carolina. However, subsequent distribution to other states may have occurred.
What is being done about the problem?
The U.S. Food and Drug Administration is advising consumers, restaurant operators, commercial shippers and processors of shellfish not to eat, serve, purchase, sell or ship oysters harvested from Area 1642 in Apalachicola Bay, Florida because the oysters may be contaminated with toxigenic Vibrio cholerae O75.
The Florida Department of Agriculture and Consumer Services Division of Aquaculture closed Area 1642 on April 29 and has asked commercial oyster harvesters and dealers who obtained oysters from this area to recall them.
The FDA is sampling oysters from Area 1642 in Apalachicola Bay as part of a reopening strategy.
Who should be contacted?
The FDA encourages consumers with questions about seafood safety to call 1-888-SAFEFOOD or to write to email@example.com.
Thursday, April 14, 2011
The U.S. Consumer Product Safety Commission (CPSC) unanimously approved (5-0) a new mandatory standard to improve the safety of toddler beds. The new federal standard builds upon the ASTM voluntary standard for toddler beds (F1821-09) and adds additional protections to prevent injuries to children.
The new federal standard requires the following:
- The upper edge of the guardrail must be at least five inches above the toddler bed's mattress.
- Spindle/slat strength testing for toddler beds must be consistent with the testing required for crib spindles/slats.
- Separate warning labels to address entrapment and strangulation hazards must appear on toddler beds.
CPSC is aware of 122 incidents from 2005 through 2010, including four deaths and 43 injuries associated with toddler beds.
Cribs that convert into toddler beds also must comply with the new federal standard for toddler beds. The mandatory standard goes into effect six months after publication in the Federal Register for toddler beds manufactured or imported on or after that date.
Congress, as part of the Consumer Product Safety Improvement Act of 2008, required the Commission to issue a mandatory standard for toddler beds, as well as other durable infant and toddler products. In addition to toddler beds, CPSC has issued mandatory standards for cribs, infant walkers and infant bath seats.