Codman & Shurtleff, Inc. / Medos S.A.
FDA adverse event reports naming Codman & Shurtleff, Inc. / Medos S.A. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: CODMAN & SHURTLEFF, INC. / MEDOS S.A..
- Total reports
- 1,737
- Deaths
- 6
- Injuries
- 1,413
- Malfunctions
- 318
Reports per year
100
402
203
104
405
1806
2507
1108
1309
34015
54616
43517
33718
Source: FDA adverse event reports by year received, 2000–2018. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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