# FDA recall Z-2499-2025

> **Physio-Control, Inc.** · Class II · device recall initiated 2025-07-22.

## Product

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 showing no signs of circulation (for example, no pulse, no coughing, or no movement).  The cprCOACHTM Feedback Technology in the LIFEPAK CR2 defibrillator is indicated for use on cardiopulmonary arrest patients and provides CPR guidance in accordance with the AHA Guidelines for patients 1 year of age or older.  The LIFEPAK CR2 defibrillator is intended for use by personnel who have been trained in its operation. Users should have received training in basic life support/AED, advanced life support, or a physician-authorized emergency medical response training program.

## Reason for recall

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

## Distribution

U.S. Nationwide distribution in the states of CO and MT.

## Key facts

- **Recall number:** Z-2499-2025
- **Recalling firm:** Physio-Control, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-07-22
- **Report date:** 2025-09-10

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Redmond, WA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2499-2025

## Citation

> AI Analytics. FDA recall Z-2499-2025. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-2499-2025. Source: US FDA. Licensed CC0.

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