Physio-Control, Inc.: Medical Device Recall in 2023 - (Recall #: Z-0301-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: September 29, 2023

Date Posted: November 22, 2023

Recall Number: Z-0301-2024

Event ID: 93233

Reason for Recall:

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

Status: Ongoing

Product Quantity: 4 units

Code Information:

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

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated