San Diego, CA (PRWEB) June 10, 2014
AttorneyOne.com, a recognized authority on law, update the website daily regarding all the latest information from the FDA on safety alerts for Infusion Pumps.
The FDA announced on May 2, that Abbott Acclaim and Hospira Acclaim Encore Infusion Pumps, by Hospira, are recalled (Class I) because broken door assemblies may result in over-infusion or delay of therapy. Use of these affected products may cause serious, life-threatening, adverse health consequences.
The affected products are:
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 Infusion Pumps 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 advises, “Hospira recommends that users inspect each Hospira/Abbott Acclaim Encore infusion pump for door handle cracks, prior to programming a therapy” by following specific steps. And the Agency adds that after following the specific steps “if you determine that a pump has a door that does not close correctly or if free flow is detected while the administration set is in the pump with the door closed, close the roller clamp, remove the pump from clinical service and call Hospira.”
AttorneyOne.com has further information on Infusion Pumps at the website including latest major drug and medical products law news.
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