Automatic External Defibrillators Categorized As A Class One Recall

AED / The Maher Law Firm and RxRecallHeartWire (3/6, Miller) reports, “The Food and Drug Administration is reminding owners of automatic external defibrillators (AEDs) to check whether their devices are subject to a January recall.” The FDA announced at that time that “certain lots of AEDs manufactured by several companies contain a defective component that may fail unexpectedly.” The recall is categorized as Class I.

Latest Recall News With RxRecall

Bookmark and Share

Comments are closed.