LIFEPAK 15 Part / Catalog Numbers / UDI-DI code: V15-7-000022 /… — Class II medical device recall Z-2497-2025
Ongoing recall by Physio-Control, Inc., reported 2025-09-10, distributed nationwide. Due to required inspections not being performed on products/units that have gone through servicing.
| Recall number | Z-2497-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Physio-Control, Inc., Redmond, WA, United States |
| Recall initiated | 2025-07-22 |
| Classified | 2025-09-02 |
| Reported by FDA | 2025-09-10 |
| Distributed | Nationwide (US) |
| Quantity | 4 units |
| UPC / GTIN / UDI-DI | 00883873871690, 00883873911631, 00883873979020, 00883873988022 |
| Serial numbers | 38154524, 39059475, 40973093, 49085553, 883873871690, 883873911631, 883873979020, 883873988022, 99577-000046, 99577-000093, 99577-001256, 99577-001957, V15-2-000051, V15-2-000099, V15-2-001603, V15-7-000022 |
Product
LIFEPAK 15 Part / Catalog Numbers / UDI-DI code: V15-7-000022 / 99577-001957 / 883873871690 V15-2-000051 / 99577-000046 / 883873988022 V15-2-000099 / 99577-000093 / 883873979020 V15-2-001603 / 99577-001256 / 883873911631 LIFEPAK 15: The LP15 is intended for use by trained medical personnel in out-of-doors and indoor emergency care settings within the environmental conditions specified in the Operating Instructions. The LP15 is designed to be used during ground transportation except when specified otherwise. Manual mode monitoring and therapy functions are intended for use on adult and pediatric patients. Automated external defibrillation mode is intended for use on patients eight years of age and older.
Reason for recall
Due to required inspections not being performed on products/units that have gone through servicing.
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-2497-2025. 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.