Zoll Medical Corp.
FDA adverse event reports naming Zoll Medical Corp. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ZOLL MEDICAL CORP..
- Total reports
- 8,218
- Deaths
- 584
- Injuries
- 80
- Malfunctions
- 7,501
Reports per year
307
4508
1609
4010
3411
712
4313
4114
615
316
317
718
819
320
121
Source: FDA adverse event reports by year received, 2007–2021. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Automated External Defibrillators (Non-Wearable)MKJ4,746
- Dc-Defibrillator, Low-Energy, (Including Paddles)LDD2,630
- Charger, PacemakerKRF459
- Electrode, Electrocardiograph, Multi-FunctionMLN216
- Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)DRO110
- Cable, Transducer And Electrode, Patient, (Including Connector)DSA30
- Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)DRT5
- Electrode, Pacemaker, TemporaryLDF5
- Aid, Cardiopulmonary ResuscitationLIX5
- Analyzer, Gas, Carbon-Dioxide, Gaseous-PhaseCCK2
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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