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LIFEPAK CR Plus and LIFEPAK Express defibrillators 80403Recalls & reported problems

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

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 00883873820513), received between Jun 4, 2019 and Jun 4, 2019 — 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.

  • MalfunctionJun 4, 2019Power Problem; Power Problem

    A 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 8667943 ↗

Sources and updates

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