LIFEPAK 15, REF: 99577-000025, 99577-000047, 99577-001256, 99577-001217, 99577-001241, 99577-001255, 99577-001219, 99577-001957, 99577-001935, 99577-001964, 99577-001955, 99577-001956, 99577-001588, 99577-001958 - Some defibrillators servic

Source: FDA | Recall date: 05/13/2026

Don't want to manually check every recall?

Track your baby products and get automatic recall alerts when something may affect your family.

Start Free Recall Tracking How Recall Alerts Work

Learn more about the baby product recall tracker, baby product recall alerts, or recall monitoring plans.

Affected product: LIFEPAK 15, REF: 99577-000025, 99577-000047, 99577-001256, 99577-001217, 99577-001241, 99577-001255, 99577-001219, 99577-001957, 99577-001935, 99577-001964, 99577-001955, 99577-001956, 99577-001588, 99577-001958

Summary: 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 inabil

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 inabil

Open Official Recall Notice Back to Home

Don't want to manually check every recall?

Track your baby products and get automatic recall alerts when something may affect your family.

Start Free Recall Tracking How Recall Alerts Work

Learn more about the baby product recall tracker, baby product recall alerts, or recall monitoring plans.