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Recall Observatory FDA recall evidence

Device product

LIFEPAK 15, REF: 99577-001955, Part Number V15-5-000584 and V15-7-000020

Z-0301-2024

September 29, 2023

Class II

Product summary

Firm
Physio-Control, Inc.
Event
Event 93233
Status
Ongoing
Classification
Class II
Quantity
4 units
Official record key
device-enforcement:Z-0301-2024

Official wording

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

Code information: UDI: 00883873871713/ Serial number: 44174756, 46013280, 46966395, 48149013

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.