This malfunction of the resuscitation bags may result in a delay of treatment and life threatening health consequences
San Diego, CA (PRWEB) May 23, 2014
AttorneyOne.com, a recognized authority on law, update the website daily regarding all the latest information from the FDA on safety alerts for resuscitator bags.
The FDA announced on May 16, that certain Ventlab Resuscitator Bags are recalled due to possible health risk. More specifically, there have been complaints regarding a sticking duckbill valve that resulted in the resuscitation bags delivering no air to the patient.
As the FDA informs, this malfunction of the resuscitation bags may result in a delay of treatment and life threatening health consequences, including hypoventilation and hypoxia, 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 resuscitator bags and inform the public. For that reason", he continues, "our focus should squarely fall on investigating these safety alerts and getting the word out.”
The US FDA recommends “Users who have resuscitation bags within the lot numbers listed in the firm's press release should stop using them and immediately contact Ventlab, LLC. for further instructions on the return of these products.” And the Agency adds “Ventlab, LLC. will notify its distributors and customers by a direct mailing and arrange for the return and replacement of all of the recalled resuscitation bags.”
AttorneyOne.com has further information on resuscitator bags at the website including latest major drug and medical products law news.
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