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
- 1,567
- Deaths
- 1
- Injuries
- 19
- Malfunctions
- 1,256
Reports per year
198
100
201
402
303
204
506
207
1308
62209
81510
9711
Source: FDA adverse event reports by year received, 1998–2011. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Stretcher, WheeledFPO1,182
- Bed, Ac-Powered Adjustable HospitalFNL180
- Stretcher, Wheeled, PoweredINK94
- Chair, Examination And TreatmentFRK58
- Mattress, Flotation Therapy, Non-PoweredIKY19
- Stool, Operating-RoomFZM15
- Table, Obstetrical, Ac-Powered (And Accessories)HDD12
- Unit, Examining/Treatment, EntETF2
- Incubator, NeonatalFMZ1
- Stretcher, Hand-CarriedFPP1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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