# FDA recall Z-1232-2025

> **Physio-Control, Inc.** · Class II · device recall initiated 2025-02-03.

## Product

LIFEPAK 20e REF 99507-000001    The AED mode is to be used only on patients in cardiopulmonary arrest.

## Reason for recall

Incorrect keypad was incorrectly installed onto a defibrillator/monitor.

## Distribution

U.S.: WV  O.U.S.: N/A

## Key facts

- **Recall number:** Z-1232-2025
- **Recalling firm:** Physio-Control, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-02-03
- **Report date:** 2025-03-05

- **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-1232-2025

## Citation

> AI Analytics. FDA recall Z-1232-2025. Retrieved 2026-07-15 from https://api.ai-analytics.org/recall/Z-1232-2025. Source: US FDA. Licensed CC0.

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