FDA Announces Recall of Alaris Pump Module: AttorneyOne Monitor and Keep Consumers Informed
On May 21, the FDA announced that the Alaris Pump model 8100, version 9.1.18, by CareFusion 303 Inc, is recalled (Class I) because the pump may have a software failure and may not properly delay an infusion. In light of this news, AttorneyOne, a recognized authority on law, updated the website providing detailed information to consumers. San Diego, CA (PRWEB) May 27, 2014 AttorneyOne.com, a recognized authority on law, update the website daily regarding all the latest information from the FDA on safety alerts for the Alaris Pump. The FDA announced on May 21, the Alaris Pump model 8100, ve
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