San Diego, CA (PRWEB) August 29, 2014
AttorneyOne.com, a recognized authority on law, update the website daily regarding all the latest information from the FDA on sterile convenience surgical packs.
The US FDA announced on August 26, that several sterile convenience surgical packs, by Customed Inc., are recalled due to potential loss of sterility.
The reason for the recall is a potential defect found due to adhesion. This defect can lead to loss of product sterility and infection. The affected products’ manufacture dates were from January 9, 2009 to May 19, 2014, and their distribution dates from January 2009 to May 2014. A detailed list of the products and lots affected is available at the FDA’s website*.
Taking into consideration the latest developments, AttorneyOne.com monitor daily and update the website providing accurate information on all relevant FDA safety alerts. Sean Burke, director of Media Relations at AttorneyOne.com, adds “we are determined to keep an eye on FDA announcements concerning sterile convenience surgical packs and inform the public. For that reason", he continues, "our focus should squarely fall on investigating these safety alerts and getting the word out.”
According to the announcement “Customers who have products should stop using the product lots included in the recall. Customed, Inc. is notifying its distributors by mail and arranging for the products return. Customed is requiring distributors to notify any customers who received the product through redistribution.”
AttorneyOne.com has further information on sterile convenience surgical packs at the website including the latest major drug, medical products, and food law news.
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