PROPAQ MDRecalls & reported problems across all models
Zoll Medical Corporation · 15 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 443
- Deaths reported
- 1
- Injuries reported
- 0
- Recalls
- 0
We found 15 models of PROPAQ MD by Zoll Medical Corporation in the FDA's device registry (GUDID). Together they are named in 443 adverse event reports in the FDA's MAUDE database, received between Aug 3, 2015 and Sep 3, 2026 — classified as 1 death, 442 malfunctions.
The most frequently reported specific device problem is “Failure of Device to Self-Test” (125 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported PROPAQ MD problems
Device problems
- Failure of Device to Self-Test125
- Failure to Power Up85
- Loss of Power30
- Pacing Problem30
- Defibrillation/Stimulation Problem29
- No Display/Image27
- Reset Problem24
- Unable to Obtain Readings24
Patient problems
- No Patient Involvement243
- No Clinical Signs, Symptoms or Conditions112
- No Information50
- No Consequences Or Impact To Patient28
- Insufficient Information8
- Death1
- Intraoperative Cardiac Valve Injury1
- Premature Labor1
PROPAQ MD models
15 models, most reported first. Each model has its own page with its reports, recalls and device details.
- PROPAQ MD 300-1011301-01Automated external defibrillators (non-wearable)1 death190 reports
- PROPAQ MD 320-2451312-01Automated external defibrillators (non-wearable)81 reports
- PROPAQ MD 310-2451312-01Automated external defibrillators (non-wearable)40 reports
- PROPAQ MD 300-1011301-01-66Automated external defibrillators (non-wearable)38 reports
- PROPAQ MD 310-2421302-01Automated external defibrillators (non-wearable)15 reports
- PROPAQ MD 310-2421312-01Automated external defibrillators (non-wearable)12 reports
- PROPAQ MD 320-2421312-01Automated external defibrillators (non-wearable)12 reports
- PROPAQ MD 320-2421302-01Automated external defibrillators (non-wearable)11 reports
- PROPAQ MD 320-2461312-01Automated external defibrillators (non-wearable)11 reports
- PROPAQ MD 310-2461312-01Automated external defibrillators (non-wearable)10 reports
- PROPAQ MD 310-2431312-01Automated external defibrillators (non-wearable)9 reports
- PROPAQ MD 300-2311301-01Automated external defibrillators (non-wearable)5 reports
- PROPAQ MD 310-2441312-01Automated external defibrillators (non-wearable)5 reports
- PROPAQ MD 320-2441312-01Automated external defibrillators (non-wearable)3 reports
- PROPAQ MD 320-2431312-01Automated external defibrillators (non-wearable)1 report
Recent PROPAQ MD adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 3, 2026Failure to Power Up
COMPLAINANT ALLEGED THAT DURING A ROUTINE SHIFT CHECK BY A CLINICIAN, THE DEVICE WOULD NOT POWER UP.COMPLAINANT INDICATED THAT THERE WAS NO PATIENT INVOLVEMENT IN THE REPORTED MALFUNCTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50592314 ↗MalfunctionAug 19, 2026Pacing Problem; Defibrillation/Stimulation Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50325182 ↗MalfunctionAug 18, 2026Unable to Obtain Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50300336 ↗MalfunctionAug 17, 2026Failure to Power Up
COMPLAINANT ALLEGED THAT DURING BIOMED TESTING, THE DEVICE WOULD NOT POWER UP. COMPLAINANT INDICATED THAT THERE WAS NO PATIENT INVOLVEMENT IN THE REPORTED MALFUNCTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50275065 ↗MalfunctionAug 10, 2026Output above Specifications
COMPLAINANT ALLEGED THAT DURING BIOMED TESTING, THE DEVICE'S DEFIB OUTPUT WAS OUT OF SPECIFICATION. COMPLAINANT INDICATED THAT THERE WAS NO PATIENT INVOLVEMENT IN THE REPORTED MALFUNCTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50199027 ↗MalfunctionJul 29, 2026Pacing Problem
COMPLAINANT ALLEGED THAT DURING BIOMED TESTING, THE DEVICE FAILED SELF-TEST FOR PACER FUNCTION. COMPLAINANT INDICATED THAT THERE WAS NO PATIENT INVOLVEMENT IN THE REPORTED MALFUNCTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50071052 ↗MalfunctionJul 15, 2026Pacing Problem; Failure of Device to Self-Test
COMPLAINANT ALLEGED THAT DURING BIOMED TESTING, THE DEVICE DISPLAYED A "PACE DEFIB DEVICE FAILURE" MESSAGE AND FAILED SELF TEST. COMPLAINANT INDICATED THAT THERE WAS NO PATIENT INVOLVEMENT IN THE REPORTED MALFUNCTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25826814 ↗MalfunctionJul 13, 2026Pacing Problem; Defibrillation/Stimulation Problem
COMPLAINANT ALLEGED THAT DURING BIOMED TESTING, THE DEVICE FAILED SELF-TEST FOR DEFIB AND PACER FUNCTIONS. COMPLAINANT INDICATED THAT THERE WAS NO PATIENT INVOLVEMENT IN THE REPORTED MALFUNCTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25796722 ↗MalfunctionJun 12, 2026Failure of Device to Self-Test
COMPLAINANT ALLEGED THAT DURING BIOMED TESTING, THE DEVICE FAILED SELF-TEST FOR PACER FUNCTION. COMPLAINANT INDICATED THAT THERE WAS NO PATIENT INVOLVEMENT IN THE REPORTED MALFUNCTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25485529 ↗MalfunctionMay 7, 2026Failure of Device to Self-Test
COMPLAINANT ALLEGED THAT DURING BIOMED TESTING, THE DEVICE FAILED SELF-TEST FOR DEFIB FUNCTION. COMPLAINANT INDICATED THAT THERE WAS NO PATIENT INVOLVEMENT IN THE REPORTED MALFUNCTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25111302 ↗MalfunctionApr 27, 2026Failure of Device to Self-Test
COMPLAINANT ALLEGED THAT DURING BIOMED TESTING, THE DEVICE FAILED SELF TEST. COMPLAINANT INDICATED THAT THERE WAS NO PATIENT INVOLVEMENT IN THE REPORTED MALFUNCTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25006781 ↗MalfunctionApr 24, 2026Failure of Device to Self-Test
COMPLAINANT ALLEGED THAT DURING BIOMED TESTING, THE DEVICE FAILED SELF TEST. COMPLAINANT INDICATED THAT THERE WAS NO PATIENT INVOLVEMENT IN THE REPORTED MALFUNCTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24981801 ↗MalfunctionApr 14, 2026Failure of Device to Self-Test
COMPLAINANT ALLEGED THAT DURING FUNCTIONAL TESTING, THE DEVICE FAILED SELF-TEST FOR DEFIB AND PACER FUNCTIONS. COMPLAINANT DID NOT INDICATE THAT THERE WAS ANY PATIENT INVOLVEMENT IN THE REPORTED MALFUNCTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24877641 ↗MalfunctionMar 3, 2026Failure to Power Up
COMPLAINANT ALLEGED THAT DURING BIOMED TESTING, THE DEVICE WOULD INTERMITTENTLY NOT POWER UP. COMPLAINANT INDICATED THAT THERE WAS NO PATIENT INVOLVEMENT IN THE REPORTED MALFUNCTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24498347 ↗MalfunctionJan 26, 2026Unable to Obtain Readings
COMPLAINANT ALLEGED THAT DURING BIOMED TESTING, THE DEVICE WAS UNABLE TO DETECT THE ATTACHED ELECTRODE PADS. COMPLAINANT INDICATED THAT THERE WAS NO PATIENT INVOLVEMENT IN THE REPORTED MALFUNCTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24179360 ↗
Other Zoll Medical Corporation products
- R SERIES94 models · 8,522 reports
- X SERIES163 models · 6,915 reports
- AED PLUS30 models · 1,966 reports · 1 recall
- Z Vent6 models · 1,204 reports · 1 recall
- Model EMV+ Vent, Army, MRI3 models · 964 reports
- E SERIES160 models · 833 reports
- ONESTEP8 models · 586 reports
- M SERIES BIPHASIC59 models · 572 reports
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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