FDA Device recall Z-0303-2024
LIFEPAK 15, REF: 99577-001957, Part Number V15-5-000586 and V15-7-000022
- FDA Device
- Class II
- ongoing
- Published 2023-11-22
On 2023-11-22 the FDA classified a Class II recall of LIFEPAK 15, REF: 99577-001957, Part Number V15-5-000586 and V15-7-000022 by Physio Control, citing their is a potential for battery pins to become loose within the defibrillator resulting in power issues.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0303-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-09-29 |
| Published | 2023-11-22 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Physio Control |
| Distribution | US |
Product
LIFEPAK 15, REF: 99577-001957, Part Number V15-5-000586 and V15-7-000022
Reason
Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.
Identifiers
| code_info | UDI: 00883873871690/ Serial number: 43393466 44142362 44739628 44742060 47821623 49025144 49663485 49887344 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0303-2024%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.