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

Recall Z-2499-2025 — LIFEPAK CR2 Part / Catalog Numbers / UDI-DI code: CR2-2-001451 99512-001434 883873785911 LIFEPAK CR2: The LIFEPAK CR2 defibrillator is indicated for use on patients 1 year of age or older in cardiopulmonary arrest. The patient must be unresponsive (unconscious), not breathing normally, and show

U.S. FDA — Device Enforcement · United States · 2025-07-22 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2499-2025
Date of alert: 2025-07-22
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Physio-Control, Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 883873785911

Reported risk: Due to required inspections not being performed on products/units that have gone through servicing.

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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