Asahi Intecc Co., Ltd.
FDA adverse event reports naming Asahi Intecc Co., Ltd. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ASAHI INTECC CO., LTD..
- Total reports
- 2,351
- Deaths
- 85
- Injuries
- 1,788
- Malfunctions
- 466
Reports per year
1912
2313
3814
8215
17416
19717
21718
23219
22120
23221
18722
14423
15324
27425
13726
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, CatheterDQX1,630
- Catheter, PercutaneousDQY620
- Guide, Wire, Catheter, NeurovasculatureMOF69
- Endoscopic Guidewire, Gastroenterology-UrologyOCY21
- Stents, Drains And Dilators For The Biliary DuctsFGE6
- Medical Device Data SystemOUG2
- Fluorometer, Lead (Dedicated Instruments)DOX1
- Catheter, Intravascular, DiagnosticDQO1
- Catheters, Transluminal Coronary Angioplasty, PercutaneousLOX1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor Asahi Intecc Co., Ltd. automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.