divendres, 5 de desembre del 2014

Philips defib updates spur ConMed electrode recall




The FDA assigns Class I recall status to several lines of ConMed's defibrillator electrodes because they won't function with a number of updated devices made by Philips.





ConMed recalls defib leads that don't work with newer Philips devices

ConMed Corp., Food & Drug Administration (FDA)

News Well, Cardiac Rhythm Management, Recalls, Regulatory/Compliance

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