Codman AND Shurtleff, Inc
FDA adverse event reports naming Codman AND Shurtleff, Inc as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: CODMAN AND SHURTLEFF, INC.
- Total reports
- 2,369
- Deaths
- 83
- Injuries
- 892
- Malfunctions
- 1,364
Reports per year
107
108
410
5511
9312
9613
23314
64415
31916
34717
20018
23619
5420
8121
222
Source: FDA adverse event reports by year received, 2007–2022. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Device, Neurovascular EmbolizationHCG961
- Intracranial Neurovascular StentNJE917
- Catheter, Continuous FlushKRA270
- Device, Vascular, For Promoting EmbolizationKRD73
- Catheter, PercutaneousDQY44
- Tissue Adhesive For Use In Embolization Of Brain Arteriovenous MalformationsKGG39
- Pump, Infusion, Implanted, ProgrammableLKK26
- Wire, Guide, CatheterDQX8
- Agent, Injectable, EmbolicMFE8
- Guide, Wire, Catheter, NeurovasculatureMOF7
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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