Physio-Control, Inc.: Medical Device Recall in 2023 - (Recall #: Z-0567-2024)

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:

AC Power Adapter for use with the LIFEPAK 15 Monitor/Defibrillator, REF: 11140-000098

Product Classification:

Class II

Date Initiated: November 6, 2023

Date Posted: December 27, 2023

Recall Number: Z-0567-2024

Event ID: 93234

Reason for Recall:

AC Power Adapter (ACPA) may not charge the monitor/defibrillator batteries and may not allow the monitor/defibrillator to power on while plugged into the ACPA.

Status: Ongoing

Product Quantity: 18,732

Code Information:

UDI-DI: 00883873940204, Adapters manufactured between 11/3/2021 - 4/24/2023

Distribution Pattern:

US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY.

Voluntary or Mandated:

Voluntary: Firm initiated