AC Power Adapter for use with the LIFEPAK 15 Monitor/Defibrillator — Class II medical device recall Z-0567-2024
Ongoing recall by Physio-Control, Inc., reported 2023-12-27, distributed nationwide. AC Power Adapter (ACPA) may not charge the monitor/defibrillator batteries and may not allow the monitor/defib
| Recall number | Z-0567-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Physio-Control, Inc., Redmond, WA, United States |
| Recall initiated | 2023-11-06 |
| Classified | 2023-12-15 |
| Reported by FDA | 2023-12-27 |
| Distributed | Nationwide (US) |
| Quantity | 18,732 |
| UPC / GTIN / UDI-DI | 00883873940204 |
| Model numbers | 11140-000098 |
Product
AC Power Adapter for use with the LIFEPAK 15 Monitor/Defibrillator, REF: 11140-000098
Reason for recall
AC Power Adapter (ACPA) may not charge the monitor/defibrillator batteries and may not allow the monitor/defibrillator to power on while plugged into the ACPA.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0567-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.