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LIFEPAK® 1000 defibrillator 97425Recalls & reported problems

Physio-Control, Inc. · USED LP1000 UNIT1000AAAAAAAACAAAAAAAAAAA · Class 3

All models of LIFEPAK 1000 defibrillator (5)

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 00883873869567), received between Mar 14, 2023 and Mar 14, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Connection 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

  • Connection Problem1

Patient problems

  • Cardiac Arrest1

Recent adverse event reports

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

  • MalfunctionMar 14, 2023Connection Problem; Connection Problem

    THE CUSTOMER CONTACTED STRYKER TO REPORT THAT DURING A CARDIAC ARREST THEIR DEVICE STATED "CHECK ELECTRODES". IN THIS STATE THE DEVICE MAY NOT BE ABLE TO DELIVER DEFIBRILLATION THERAPY IF NEEDED. THE PATIENT ASSOCIATED WITH THE REPORTED EVENT DID NOT SURVIVE. THERE HAS BEEN NO ALLEGED DEVICE CONTRIBUTION TO THE PATIENT OUTCOME, HOWEVER A DELAY WAS REPORTED.

    Patient problems: Cardiac Arrest

    MAUDE report 16542081 ↗

Other Automated external defibrillators (non-wearable) devices

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Sources and updates

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