Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1896-2012 — Philips HeartStart MRx monitor/defibrillators Models: M3535A, M3536A, M3536M4, M3536M5, and M3536M6 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 opera

U.S. FDA — Device Enforcement · United States · 2012-06-20 · Class II

AI-assisted, human-edited — this page is drafted with AI from public-source data, then reviewed before publication. How we use AI →

Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1896-2012
Date of alert: 2012-06-20
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Philips Healthcare Inc.
Product category: device
Product type: Devices

Reported risk: HeartStart MRx Unexpected Pads/Paddles ECG Failure

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

Related