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
- 2,377
- Deaths
- 85
- Injuries
- 1,808
- Malfunctions
- 471
Reports per year
1912
2313
3814
8215
17416
19717
21718
23219
22120
23221
18722
14423
15324
27425
16326
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Wire, Guide, CatheterDQX1,645
- Catheter, PercutaneousDQY629
- Guide, Wire, Catheter, NeurovasculatureMOF71
- 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.
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