Integra Lifesciences Mansfield
FDA adverse event reports naming Integra Lifesciences Mansfield as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: INTEGRA LIFESCIENCES MANSFIELD.
- Total reports
- 1,753
- Deaths
- 11
- Injuries
- 988
- Malfunctions
- 754
Reports per year
719
6220
13321
21722
23223
52524
40125
17626
Source: FDA adverse event reports by year received, 2019–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Shunt, Central Nervous System And ComponentsJXG693
- Device, Monitoring, Intracranial PressureGWM503
- Drills, Burrs, Trephines & Accessories (Compound, Powered)HBF281
- Unit, Cryosurgical, AccessoriesGEH46
- Neurosurgical PaddieHBA46
- Electrosurgical, Cutting & Coagulation & AccessoriesGEI41
- Coagulator-Cutter, Endoscopic, Unipolar (And Accessories)KNF16
- Laparoscope, General & Plastic SurgeryGCJ15
- HemostatHRQ8
- Instrument, Manual, Surgical, General UseMDM7
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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