LIFEPAK 15, REF: 99577-001957, Part Number V15-5-000586 and V15-7-000022
Reported: November 22, 2023 Initiated: September 29, 2023 #Z-0303-2024
Product Description
LIFEPAK 15, REF: 99577-001957, Part Number V15-5-000586 and V15-7-000022
Reason for Recall
Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.
Details
- Recalling Firm
- Physio-Control, Inc.
- Units Affected
- 8 units
- Distribution
- US Nationwide distribution in the states of AZ, CA, NC, NJ, NY.
- Location
- Redmond, WA
Frequently Asked Questions
What product was recalled? ▼
LIFEPAK 15, REF: 99577-001957, Part Number V15-5-000586 and V15-7-000022. Recalled by Physio-Control, Inc.. Units affected: 8 units.
Why was this product recalled? ▼
Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on November 22, 2023. Severity: Moderate. Recall number: Z-0303-2024.
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