Clearstream Technologies Ltd.
FDA adverse event reports naming Clearstream Technologies Ltd. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: CLEARSTREAM TECHNOLOGIES LTD..
- Total reports
- 2,371
- Deaths
- 23
- Injuries
- 319
- Malfunctions
- 2,027
Reports per year
412
113
114
915
4116
15417
18118
15319
15620
24821
28522
27823
35124
33125
17626
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
- Iliac Covered Stent, ArterialPRL1,166
- Catheter, Angioplasty, Peripheral, TransluminalLIT515
- Percutaneous Catheter For Creation Of An Arteriovenous Fistula For Hemodialysis AccessPQK314
- Introducer, CatheterDYB296
- Catheter, PercutaneousDQY56
- Device, Vascular, For Promoting EmbolizationKRD16
- Stent, IliacNIO4
- Port & Catheter, Implanted, Subcutaneous, IntravascularLJT3
- Electrosurgical, Cutting & Coagulation & AccessoriesGEI1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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