# FDA recall Z-0296-2024

> **Physio-Control, Inc.** · Class II · device recall initiated 2023-09-29.

## Product

LIFEPAK 15, REF: 99577-000046, Part Number V15-2-000051

## Reason for recall

Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.

## Distribution

US Nationwide distribution in the states of AZ, CA, NC, NJ, NY.

## Key facts

- **Recall number:** Z-0296-2024
- **Recalling firm:** Physio-Control, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-09-29
- **Report date:** 2023-11-22

- **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-0296-2024

## Citation

> AI Analytics. FDA recall Z-0296-2024. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-0296-2024. Source: US FDA. Licensed CC0.

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