Skip to content

LIFEPAK® CR Plus and LIFEPAK Express defibrillators 80403 (REF 80403-000149)Recalls & reported problems

Physio-Control, Inc. · PACKAGE,LPCR PLUS,AUTO,ENGLISH,AHA2005 · Class 3

All models of LIFEPAK CR Plus and LIFEPAK Express defibrillators (25)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00885074440156), received between Apr 24, 2018 and Apr 24, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Power Problem” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Power Problem1

Patient problems

  • No Patient Involvement1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionApr 24, 2018Power Problem; Power Problem

    THE CUSTOMER CONTACTED PHYSIO-CONTROL TO REPORT THAT THEIR DEVICE WAS SHOWING ALL THREE ICONS (ATTENTION, CHARGE-PAK AND SERVICE WRENCH). WITH ALL THREE ICONS ILLUMINATED, THE DEVICE MAY NOT HAVE SUFFICIENT POWER AVAILABLE TO DELIVER EFFECTIVE DEFIBRILLATION THERAPY TO A PATIENT, IF IT WAS NEEDED. THERE WAS NO PATIENT USE ASSOCIATED WITH THE REPORTED EVENT.

    Patient problems: No Patient Involvement

    MAUDE report 7456671 ↗

Other Automated external defibrillators (non-wearable) devices

All Automated external defibrillators (non-wearable) devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page