Av-temecula-ct
FDA adverse event reports naming Av-temecula-ct as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: AV-TEMECULA-CT.
- Total reports
- 77,603
- Deaths
- 2,495
- Injuries
- 48,755
- Malfunctions
- 26,353
Reports per year
208
409
21010
8,84411
8,27912
8,40813
8,57514
8,02915
9,42516
10,15917
10,08718
5,58119
Source: FDA adverse event reports by year received, 2008–2019. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Device, Hemostasis, VascularMGB28,402
- Coronary Drug-Eluting StentNIQ17,022
- Catheters, Transluminal Coronary Angioplasty, PercutaneousLOX8,562
- Mitral Valve Repair DevicesNKM5,911
- Stent, CoronaryMAF4,050
- Wire, Guide, CatheterDQX3,207
- Catheter, Angioplasty, Peripheral, TransluminalLIT2,737
- Stent, Superficial Femoral ArteryNIP1,189
- Stent, CarotidNIM1,156
- Catheter, SteerableDRA1,146
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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