William Cook Europe
FDA adverse event reports naming William Cook Europe as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: WILLIAM COOK EUROPE.
- Total reports
- 14,372
- Deaths
- 305
- Injuries
- 10,226
- Malfunctions
- 3,759
Reports per year
3812
3713
8214
17815
1,41316
2,39917
1,47718
2,82719
1,54120
2,11021
1,12822
33323
29724
28225
12426
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
- Filter, Intravascular, CardiovascularDTK12,535
- System, Endovascular Graft, Aortic Aneurysm TreatmentMIH1,604
- Wire, Guide, CatheterDQX74
- Device, Vascular, For Promoting EmbolizationKRD49
- Tube, Tracheal (W/Wo Connector)BTR45
- Introducer, CatheterDYB20
- Instrument, Ent Manual SurgicalLRC18
- Stent, RenalNIN16
- Tube, Tracheal/Bronchial, Differential Ventilation (W/Wo Connector)CBI2
- Free Radical Assay, OpiatesDKT2
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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