# FDA recall Z-2497-2025

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

## Product

LIFEPAK 15 Part / Catalog Numbers / UDI-DI code:  V15-7-000022	 / 99577-001957 / 883873871690  V15-2-000051 / 99577-000046 / 883873988022  V15-2-000099 / 99577-000093 / 883873979020  V15-2-001603 / 99577-001256 / 883873911631    LIFEPAK 15: The LP15 is intended for use by trained medical personnel in out-of-doors and indoor emergency care settings within the environmental conditions specified in the Operating Instructions. The LP15 is designed to be used during ground transportation except when specified otherwise. Manual mode monitoring and therapy functions are intended for use on adult and pediatric patients. Automated external defibrillation mode is intended for use on patients eight years of age and older.

## 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-2497-2025
- **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-2497-2025

## Citation

> AI Analytics. FDA recall Z-2497-2025. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-2497-2025. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*