LIFEPAK 20e REF 99507-000001 The AED mode is to be used only on… — Class II medical device recall Z-1232-2025
Ongoing recall by Physio-Control, Inc., reported 2025-03-05, distributed in WV. Incorrect keypad was incorrectly installed onto a defibrillator/monitor.
| Recall number | Z-1232-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Physio-Control, Inc., Redmond, WA, United States |
| Recall initiated | 2025-02-03 |
| Classified | 2025-02-25 |
| Reported by FDA | 2025-03-05 |
| Distributed | WV |
| Quantity | 1 |
| UPC / GTIN / UDI-DI | 00883873813751 |
| Serial numbers | 38289467 |
| Model numbers | 99507-000001 |
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.
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-1232-2025. 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.