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

Recall Z-1931-2019 — ZOLL AED PRO Automated External Defibrillator Product Usage: The AED PRO unit is intended to defibrillate victims of ventricular fibrillation or pulseless ventricular tachycardia, for ECG monitoring, and for CPR monitoring of patients. The CPR monitoring function provides a metronome designed to

U.S. FDA — Device Enforcement · United States · 2019-06-12 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1931-2019
Date of alert: 2019-06-12
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: ZOLL Medical Corporation
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 00847946016128

Reported risk: There is a potential for the device to fail to deliver energy to the patient.

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.

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