FDA Warns Of Possible Philips Defibrillator Failure
The agency issued a safety communication on HeartStart automated external defibrillator products made by Philips Medical Systems, part of the medical device unit of Koninklijke Philips NV. The advisory follows a massive recall of the devices initiated by Philips last year, covering around 700,000 devices.
The FDA warned that the devices may falter...
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