Lifepak 15 recall
LIFEPAK 15, REF: 99577-001255, Part Number V15-2-001602
Why was Lifepak 15 recalled?
Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI: 00883873911648/ Serial number: 40644322 40644323 40644331 42221204 42934131
- Product
- LIFEPAK 15, REF: 99577-001255, Part Number V15-2-001602
- Recalling firm
- Physio-Control, Inc.
- Quantity
- 5 units
- Distribution
- US Nationwide distribution in the states of AZ, CA, NC, NJ, NY.
- Recall date
- November 22, 2023
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)