FDAJuly 12, 2017device

MRx Defibrillator Model # M3535A & M3536A, UDI 00884838000018(21)US00601969 Product Usage: The HeartStart MRx is for use for the termination of ventricular tachycardia and ventricular fibrillation. The device is for use by qualified medical personnel trained in the operation of the device and qua...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Affected units may have a defective component that is intended to protect the internal circuitry from high voltages during shock delivery. The defective component may also prevent delivery of shocks in AED mode.

What to do

FDA enforcement status: Terminated

Brands named

philips north americaphilipsphilips north

UPCs

00884838000018

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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