Stryker Medical
FDA adverse event reports naming Stryker Medical as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: STRYKER MEDICAL.
- Total reports
- 26,310
- Deaths
- 24
- Injuries
- 322
- Malfunctions
- 25,686
Reports per year
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Bed, Ac-Powered Adjustable HospitalFNL13,431
- Stretcher, WheeledFPO9,159
- Stretcher, Wheeled, PoweredINK2,150
- Table, Obstetrical, Ac-Powered (And Accessories)HDD623
- Mattress, Flotation Therapy, Non-PoweredIKY320
- Stretcher, Hand-CarriedFPP164
- Bed, Pediatric Open HospitalFMS126
- Chair, Examination And TreatmentFRK71
- Mattress, Air Flotation, Alternating PressureFNM61
- Stool, Operating-RoomFZM53
Recent recalls
- 2026-03-19Open, ClassifiedUnder Investigation by firm
Cub Pediatric Crib, Model FL19H
Cribs sold in the USA are missing two access door warning labels.
- 2025-12-11Open, ClassifiedRelease of Material/Component prior to receiving test results
Stryker MV3 bariatric bed, Part Number 5900000001
Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX mattresses because some of these products have been sold in close proximity, suggesting a potential intent for them to be used together. These products have not been tested for compatibility and thus are not designed to be used together. The combination of both is not recommended by Stryker.
- 2025-12-11Open, ClassifiedRelease of Material/Component prior to receiving test results
Stryker Arise 1000EX mattress, Part Number 2236000000
Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX mattresses because some of these products have been sold in close proximity, suggesting a potential intent for them to be used together. These products have not been tested for compatibility and thus are not designed to be used together. The combination of both is not recommended by Stryker.
- 2023-12-01Open, ClassifiedProcess control
ProCuity bed series, model number 3009, item number: 300900000000,
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
- 2023-12-01Open, ClassifiedProcess control
ProCuity bed series, model number 3009, item number: 3009PX-L-100.
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
- 2023-12-01Open, ClassifiedProcess control
ProCuity bed series, model number 3009, item number: 3009PX-L-200
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
- 2023-12-01Open, ClassifiedProcess control
ProCuity bed series, model number 3009, item number: 3009PX-LE-400.
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
- 2023-12-01Open, ClassifiedProcess control
ProCuity bed series, model number 3009, item number: 3009PX-LE-450.
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
- 2023-12-01Open, ClassifiedProcess control
ProCuity bed series, model number 3009, item number: 3009PX-LEX-400.
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
- 2023-12-01Open, ClassifiedProcess control
ProCuity bed series, model number 3009, item number: 3009PX-LEX-450.
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
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