Stryker Corp., Medical Division
FDA adverse event reports naming Stryker Corp., Medical Division as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: STRYKER CORP., MEDICAL DIVISION.
- Total reports
- 1,750
- Deaths
- 2
- Injuries
- 45
- Malfunctions
- 1,568
Reports per year
299
401
2002
203
604
105
1506
6907
6008
47209
91710
18211
Source: FDA adverse event reports by year received, 1999–2011. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Stretcher, WheeledFPO778
- Bed, Ac-Powered Adjustable HospitalFNL701
- Stretcher, Wheeled, PoweredINK120
- Chair, Examination And TreatmentFRK68
- Mattress, Flotation Therapy, Non-PoweredIKY32
- Table, Obstetrical, Ac-Powered (And Accessories)HDD25
- Stool, Operating-RoomFZM18
- Stretcher, Hand-CarriedFPP5
- Bed, Pediatric Open HospitalFMS1
- Lift, Patient, Non-Ac-PoweredFSA1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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