Physio-Control, Inc.: Medical Device Recall in 2025 - (Recall #: Z-2497-2025)

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 15 Part / Catalog Numbers / UDI-DI code: V15-7-000022 / 99577-001957 / 883873871690 V15-2-000051 / 99577-000046 / 883873988022 V15-2-000099 / 99577-000093 / 883873979020 V15-2-001603 / 99577-001256 / 883873911631 LIFEPAK 15: The LP15 is intended for use by trained medical personnel in out-of-doors and indoor emergency care settings within the environmental conditions specified in the Operating Instructions. The LP15 is designed to be used during ground transportation except when specified otherwise. Manual mode monitoring and therapy functions are intended for use on adult and pediatric patients. Automated external defibrillation mode is intended for use on patients eight years of age and older.

Product Classification:

Class II

Date Initiated: July 22, 2025

Date Posted: September 10, 2025

Recall Number: Z-2497-2025

Event ID: 96949

Reason for Recall:

Due to required inspections not being performed on products/units that have gone through servicing.

Status: Ongoing

Product Quantity: 4 units

Code Information:

Part / Catalog Numbers / UDI-DI code / Serial Number: V15-7-000022 / 99577-001957 / 883873871690 / 49085553 V15-2-000051 / 99577-000046 / 883873988022 / 38154524 V15-2-000099 / 99577-000093 / 883873979020 / 39059475 V15-2-001603 / 99577-001256 / 883873911631 / 40973093

Distribution Pattern:

U.S. Nationwide distribution in the states of CO and MT.

Voluntary or Mandated:

Voluntary: Firm initiated