# FDA recall Z-0230-2025

> **Physio-Control, Inc.** · Class II · device recall initiated 2024-08-30.

## Product

LIFEPAK 15 (LP15) Model/Catalog Numbers:  o 97577-000101  o 99577-000046  o 99577-000055  o 99577-000061  o 99577-000076  o 99577-001250  o 99577-001255  o 99577-001256  o 99577-001368  o 99577-001955  o 99577-001956  o 99577-001957  o 99577-001958  o 99577-001962  LIFEPAK 15 intended use monitor/defibrillator.

## Reason for recall

Due to an out of tolerance tool being used on monitor/defibrillator systems.

## Distribution

U.S.: CT, GA, MA, NY, OH, WA, and WV.  O.U.S.: N/A

## Key facts

- **Recall number:** Z-0230-2025
- **Recalling firm:** Physio-Control, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-08-30
- **Report date:** 2024-11-06

- **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-0230-2025

## Citation

> AI Analytics. FDA recall Z-0230-2025. Retrieved 2026-08-23 from https://api.ai-analytics.org/recall/Z-0230-2025. Source: US FDA. Licensed CC0.

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