Official recall notice
FDA DeviceClass IINotable
FDA Recall: LIFEPAK 15, REF: 99577-000025, 99577-000047, 99577-001256, 99577-001217, 99577-001241, 99577-001255,
- Recall date
- 2026-05-13
- Brand
- Physio-Control, Inc.
- Category
- Medical Device
- FDA class
- Class II
Why it was recalled
Hazard
Some defibrillators serviced between July 2023 through November 2025 were serviced without objective evidence that a Performance Inspection Procedure (PIP) was conducted, and the inability to perform the device's intended use may result in potential harms such as delays or inability to provide therapy.
Recommended action
What to do
206
Product description
Some defibrillators serviced between July 2023 through November 2025 were serviced without objective evidence that a Performance Inspection Procedure (PIP) was conducted, and the inability to perform the device's intended use may result in potential harms such as delays or inability to provide therapy.