Physio-Control, Inc.: Medical Device Recall in 2025 - (Recall #: Z-1232-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

LIFEPAK 20e REF 99507-000001 The AED mode is to be used only on patients in cardiopulmonary arrest.

Product Classification:

Class II

Date Initiated: February 3, 2025

Date Posted: March 5, 2025

Recall Number: Z-1232-2025

Event ID: 96095

Reason for Recall:

Incorrect keypad was incorrectly installed onto a defibrillator/monitor.

Status: Ongoing

Product Quantity: 1

Code Information:

Model/Catalog Number: 99507-000001 UDI-DI code: 00883873813751 Serial Number: 38289467

Distribution Pattern:

U.S.: WV O.U.S.: N/A

Voluntary or Mandated:

Voluntary: Firm initiated