DEVICE SPOTLIGHT
- DEVICE NAMES: MESH, SURGICAL, POLYMERIC; MESH, SURGICAL
- PRODUCT CODES: FTL, FTM
ADVERSE EVENTS RECEIVED BY THE FDA
- Total Reports: 51,844
- Injury Reports: 48,974
- Malfunction Reports: 2,209
- Death Reports: 388
- Other: 273
- RECALLS: 27
IMPROVE OUTCOMES | REDUCE RISK
DEVICE SPOTLIGHT
ADVERSE EVENTS RECEIVED BY THE FDA
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