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Recall Observatory FDA recall evidence

Device product

LIFEPAK 15, REF: 99577-001255, Part Number V15-2-001602

Z-0299-2024

September 29, 2023

Class II

Product summary

Firm
Physio-Control, Inc.
Event
Event 93233
Status
Ongoing
Classification
Class II
Quantity
5 units
Official record key
device-enforcement:Z-0299-2024

Official wording

Reason: Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.

Code information: UDI: 00883873911648/ Serial number: 40644322 40644323 40644331 42221204 42934131

Distribution pattern: US Nationwide distribution in the states of AZ, CA, NC, NJ, NY.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.