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
- 3,254
- Deaths
- 139
- Injuries
- 54
- Malfunctions
- 3,046
Reports per year
9704
1705
4606
2507
22908
25709
42610
26111
24512
30513
20814
14515
118
119
120
Source: FDA adverse event reports by year received, 2004–2020. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Automated External Defibrillators (Non-Wearable)MKJ2,760
- Dc-Defibrillator, Low-Energy, (Including Paddles)LDD347
- Charger, PacemakerKRF56
- Electrode, Electrocardiograph, Multi-FunctionMLN51
- Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)DRO14
- Computer, Blood-PressureDSK9
- Aid, Cardiopulmonary ResuscitationLIX9
- Analyzer, Gas, Carbon-Dioxide, Gaseous-PhaseCCK2
- Compressor, Cardiac, ExternalDRM2
- Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)DRT2
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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