Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for battery pins to...

Date: September 29, 2023
Company: Physio-Control, Inc.
Status: Ongoing
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Physio-Control, Inc. directly.

Affected Products

LIFEPAK 15, REF: 99577-001958, Part Number: V15-7-000023

Quantity: 1 unit

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Physio-Control, Inc.

Physio-Control, Inc. has 38 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report