Terumo Corporation, Ashitaka
FDA adverse event reports naming Terumo Corporation, Ashitaka as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: TERUMO CORPORATION, ASHITAKA.
- Total reports
- 3,847
- Deaths
- 54
- Injuries
- 1,676
- Malfunctions
- 2,091
Reports per year
6612
14713
25914
26315
31816
25917
26018
25419
30620
28521
28222
18623
18024
33525
17526
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Wire, Guide, CatheterDQX1,383
- Oxygenator, Cardiopulmonary BypassDTZ1,355
- Catheter, Intravascular, DiagnosticDQO216
- Introducer, CatheterDYB190
- Clamp, VascularDXC172
- Stent, Superficial Femoral ArteryNIP119
- Endoscopic Guidewire, Gastroenterology-UrologyOCY118
- Catheter, PercutaneousDQY81
- Dialyzer, Capillary, Hollow FiberFJI59
- Catheter, Continuous FlushKRA48
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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