FDAFDA · Food and drugs·Recall number Z-0303-2024
LIFEPAK 15, REF: 99577-001957, Part Number V15-5-000586 and V15-7-000022
Published November 22, 2023 · Recall initiated: September 29, 2023
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Physio-Control, Inc.
- Distributor
- US Nationwide distribution in the states of AZ, CA, NC, NJ, NY.
- Lot
- UDI: 00883873871690/ Serial number: 43393466 44142362 44739628 44742060 47821623 49025144 49663485 49887344
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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