PRO PADZ 8900-4055-40Recalls & reported problems
Zoll Medical Corporation · PRO PADZ STERILE MULTI-FUNCTION ELECTRODES WITH 10 FOOT LEAD WIRES - 1 PAIR · Class 3
All models of PRO PADZ (6)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00847946016487), received between Dec 7, 2020 and Apr 20, 2022 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Failure to Convert Rhythm” (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
- Failure to Convert Rhythm1
- Failure to Deliver Shock/Stimulation1
- Noise, Audible1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 20, 2022Failure to Deliver Shock/Stimulation; Failure to Convert Rhythm; Failure to Deliver Shock/Stimulation; Failure to Convert Rhythm
COMPLAINANT ALLEGED THAT WHILE ATTEMPTING TO TREAT A (B)(6)-YEAR-OLD MALE PATIENT, THE DEVICE FAILED TO DISCHARGE. COMPLAINANT INDICATED THE CLINICIAN SWITCHED TO PADDLES TO CONTINUE TREATING THE PATIENT. COMPLAINANT INDICATED THAT THERE WAS NO ADVERSE EFFECT TO THE PATIENT DUE TO THE REPORTED MALFUNCTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14161941 ↗MalfunctionDec 7, 2020Noise, Audible; Noise, Audible
COMPLAINANT ALLEGED THAT WHILE ATTEMPTING TO DEFIBRILLATE A PATIENT (AGE & GENDER UNKNOWN), A LOUD POP NOISE WAS HEARD. COMPLAINANT INDICATED THAT THERE WAS NO ADVERSE EFFECT TO THE PATIENT DUE TO THE REPORTED MALFUNCTION.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10962540 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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