ZOLL BATTERY SLA 1001-0144Recalls & reported problems
Zoll Medical Corporation · Class 3
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00847946016678), received between Dec 18, 2017 and Apr 14, 2022 — classified as 2 injuries.
The most frequently reported specific device problem is “Loss of Power” (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
- Loss of Power1
- Noise, Audible1
Patient problems
- No Information1
- Tinnitus1
- Total Hearing Loss1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryApr 14, 2022Noise, Audible; Noise, Audible
COMPLAINANT ALLEGED THAT A BATTERY CHARGE WAS TO BE CARRIED OUT WITH THE ASSOCIATED CHARGING STATION. WHEN INSERTING THE BATTERY INTO THE CHARGING STATION, WHICH WAS ALREADY UNDER POWER, THERE WAS A LOUD BANG AND THE CAP, WHICH WAS ATTACHED TO THE BATTERY, CAME LOOSE AND FLEW OFF. COMPLAINANT INDICATED THE EMPLOYEE SUFFERED HEARING LOSS AND TINNITUS ON BOTH SIDES. THE EMPLOYEE WAS THEN SEEN BY AN EAR NOSE AND THROAT SPECIALIST.
Patient problems: Tinnitus; Total Hearing Loss
MAUDE report 14115602 ↗InjuryDec 18, 2017Loss of Power; Loss of Power
COMPLAINANT ALLEGED THAT WHILE ATTEMPTING TO TREAT A PATIENT (AGE & GENDER UNKNOWN), THE DEVICE INAPPROPRIATELY SHUT DOWN. COMPLAINANT INDICATED THAT THE PATIENT SUSTAINED A SERIOUS INJURY.
Patient problems: No Information
MAUDE report 7126391 ↗
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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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