Integra Lifesciences Corporation Oh/usa
FDA adverse event reports naming Integra Lifesciences Corporation Oh/usa as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: INTEGRA LIFESCIENCES CORPORATION OH/USA.
- Total reports
- 5,667
- Deaths
- 6
- Injuries
- 1,286
- Malfunctions
- 4,374
Reports per year
19312
20513
18614
26715
39316
33117
29618
1,09019
91520
72721
29022
24023
17924
24525
8426
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Holder, Head, Neurosurgical (Skull Clamp)HBL3,934
- Operating Room Accessories Table TrayFWZ952
- DermatomeGFD251
- Neurological Stereotaxic InstrumentHAW71
- Retractor, Self-RetainingFFO55
- Headrest, NeurosurgicalHBM51
- Expander, Surgical, Skin GraftFZW40
- Retractor, Self-Retaining, For NeurosurgeryGZT40
- Accessories, ArthroscopicNBH36
- RetractorGAD33
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor Integra Lifesciences Corporation Oh/usa automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.