Stryker Corp., Medical DIV.
FDA adverse event reports naming Stryker Corp., Medical DIV. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: STRYKER CORP., MEDICAL DIV..
- Total reports
- 2,297
- Deaths
- 6
- Injuries
- 32
- Malfunctions
- 2,182
Reports per year
301
102
103
104
1205
4006
1307
1408
11709
1,65110
44411
Source: FDA adverse event reports by year received, 2001–2011. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Bed, Ac-Powered Adjustable HospitalFNL1,305
- Stretcher, WheeledFPO619
- Stretcher, Wheeled, PoweredINK214
- Table, Obstetrical, Ac-Powered (And Accessories)HDD82
- Chair, Examination And TreatmentFRK33
- Stretcher, Hand-CarriedFPP12
- Stool, Operating-RoomFZM12
- Mattress, Flotation Therapy, Non-PoweredIKY11
- Bed, Pediatric Open HospitalFMS5
- Mattress, Air Flotation, Alternating PressureFNM2
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor Stryker Corp., Medical DIV. 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.