Zoll Manufacturing Corporation
FDA adverse event reports naming Zoll Manufacturing Corporation as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ZOLL MANUFACTURING CORPORATION.
- Total reports
- 134,118
- Deaths
- 3,475
- Injuries
- 38,304
- Malfunctions
- 92,335
Reports per year
4213
3,07414
8,16915
9,45916
10,85117
9,93918
9,89819
11,97220
12,53121
12,74422
13,06523
12,85724
12,48725
7,03026
Source: FDA adverse event reports by year received, 2013–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Wearable Automated External DefibrillatorMVK131,938
- Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)MHX2,165
- Automated External Defibrillators (Non-Wearable)MKJ6
- Laser, Dental, Soft TissueNVK4
- Detector And Alarm, ArrhythmiaDSI3
- Implantable Cardioverter Defibrillator (Non-Crt)LWS1
- Lens, Intraocular, AccommodativeNAA1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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