FMCClass 1
Patient Examination Glove
FDA adverse event reports and recall history for patient examination glove (product code FMC), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 484
- Deaths
- 1
- Injuries
- 30
- Malfunctions
- 431
Reports per year
907
508
309
710
111
212
313
714
4115
33316
3217
119
120
321
125
Source: FDA adverse event reports by year received, 2007–2025. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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