LIFEPAK 15 — Class II medical device recall Z-0305-2024
Ongoing recall by Physio-Control, Inc., reported 2023-11-22, distributed nationwide. Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.
| Recall number | Z-0305-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Physio-Control, Inc., Redmond, WA, United States |
| Recall initiated | 2023-09-29 |
| Classified | 2023-11-14 |
| Reported by FDA | 2023-11-22 |
| Distributed | Nationwide (US) |
| Quantity | 2 units |
| UPC / GTIN / UDI-DI | 00883873871669 |
| Serial numbers | 48433670, 48744028 |
| Model numbers | 99577-001960, V15-7-000026 |
Product
LIFEPAK 15, REF: 99577-001960, Part Number: V15-7-000026
Reason for recall
Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.
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-0305-2024. 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.