we are determined to keep an eye on FDA announcements concerning LifeCare Flexible Intravenous Solutions and inform the public
San Diego, CA (PRWEB) October 21, 2014
AttorneyOne.com, a recognized authority on law, update the website daily regarding all the latest information from the FDA on LifeCare Flexible Intravenous Solutions.
The US FDA announced on October 15, that certain lots of LifeCare Flexible Intravenous Solutions by Hospira, Inc. are recalled due to potential for leakage.
The reason for the recall is that during re-inspection of a manufactured product lot a single puncture mark was identified going through the overwrap and primary container. This may cause a leakage with the potential for contamination, compromised sterility, inadequate or inconsistent solution/medication dosing, and/or delay in therapy, drug waste, spillage, that may require medical intervention. Moreover, if a hazardous drug is used, hazardous topical exposure may occur.
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 LifeCare Flexible Intravenous Solutions and inform the public. For that reason," he continues, "our focus should squarely fall on investigating these safety alerts and getting the word out.”
As the FDA recommends “Anyone with an existing inventory of the recalled lots should stop use and distribution and quarantine the product immediately.” And the Agency adds “Hospira will be notifying its direct customers via a recall letter and will arrange for impacted product to be returned to Stericycle.”
AttorneyOne.com has further information on LifeCare Flexible Intravenous Solutions at the website including the latest major drug, food, and medical products law news.
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