BfArM - Federal Institute for Drugs and Medical Devices

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Product group Medical electronics / Electromedical devices
Reference 03756/09

The Philips Medical Systems has issued a Field Safety Notice concerning a corrective action of the automated external defibrillator (AED) HeartStart FR2+ model nos M3840A, M3841A, M3860A and M3861A. A memory chip that has a higher than expected failure rate could render the AED inoperable. The affected devices will be replaced.

Recall for HeartStart FR2, Philips , Download_VeroeffentlichtAm_EN PDF, 95KB, File does not meet accessibility standards