Maquet CV
FDA adverse event reports naming Maquet CV as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: MAQUET CV.
- Total reports
- 4,465
- Deaths
- 3
- Injuries
- 229
- Malfunctions
- 4,231
Reports per year
42415
1,30316
1,13317
1,30818
29719
Source: FDA adverse event reports by year received, 2015–2019. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Electrosurgical, Cutting & Coagulation & AccessoriesGEI2,916
- Clamp, VascularDXC948
- Laparoscope, General & Plastic SurgeryGCJ154
- Stabilizer, HeartMWS147
- Lavage, JetFQH126
- Unit, Cautery, Thermal, Ac-PoweredHQO100
- Prosthesis, Vascular Graft, Of 6mm And Greater DiameterDSY19
- Instruments, Surgical, CardiovascularDWS16
- Cutter, SurgicalFZT16
- Graft, Vascular, Synthetic/Biologic CompositeMAL16
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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