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Stryker Medical Division of Stryker Recalls
80 recalls on record · July 4, 2012 to March 25, 2026 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
March 25, 2026Medical DevicesFDA
Stryker Medical Division of Stryker Corporation recalls Cub Pediatric Crib, Model FL19H
Hazard: Cribs sold in the USA are missing two access door warning labels.
December 17, 2025Medical DevicesFDA
Stryker Medical Division of Stryker Corporation recalls Stryker Arise 1000EX mattress, Part Number 2236000000
Hazard: 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.
December 17, 2025Medical DevicesFDA
Stryker Medical Division of Stryker Corporation recalls Stryker MV3 bariatric bed, Part Number 5900000001
Hazard: 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.
December 13, 2023Medical DevicesFDA
Stryker Medical Division of Stryker Corporation recalls ProCurity bed series, model number 3009, item number: 3009PX-ZX-450.
Hazard: Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
December 13, 2023Medical DevicesFDA
Stryker Medical Division of Stryker Corporation recalls ProCurity bed series, model number 3009, item number: 3009PX-ZMX-600.
Hazard: Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
December 13, 2023Medical DevicesFDA
Stryker Medical Division of Stryker Corporation recalls ProCurity bed series, model number 3009, item number: 3009PX-ZMX-450.
Hazard: Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
December 13, 2023Medical DevicesFDA
Stryker Medical Division of Stryker Corporation recalls ProCuity bed series, model number 3009, item number: 3009PX-ZM-600.
Hazard: Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
December 13, 2023Medical DevicesFDA
Stryker Medical Division of Stryker Corporation recalls ProCuity bed series, model number 3009, item number: 3009PX-ZM-450.
Hazard: Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
December 13, 2023Medical DevicesFDA
Stryker Medical Division of Stryker Corporation recalls ProCuity bed series, model number 3009, item number: 3009PX-Z-450.
Hazard: Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
December 13, 2023Medical DevicesFDA
Stryker Medical Division of Stryker Corporation recalls ProCuity bed series, model number 3009, item number: 3009PX-LEX-450.
Hazard: Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
December 13, 2023Medical DevicesFDA
Stryker Medical Division of Stryker Corporation recalls ProCuity bed series, model number 3009, item number: 3009PX-LEX-400.
Hazard: Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
December 13, 2023Medical DevicesFDA
Stryker Medical Division of Stryker Corporation recalls ProCuity bed series, model number 3009, item number: 3009PX-LE-450.
Hazard: Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
December 13, 2023Medical DevicesFDA
Stryker Medical Division of Stryker Corporation recalls ProCuity bed series, model number 3009, item number: 3009PX-LE-400.
Hazard: Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
December 13, 2023Medical DevicesFDA
Stryker Medical Division of Stryker Corporation recalls ProCuity bed series, model number 3009, item number: 3009PX-L-200
Hazard: Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
December 13, 2023Medical DevicesFDA
Stryker Medical Division of Stryker Corporation recalls ProCuity bed series, model number 3009, item number: 3009PX-L-100.
Hazard: Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
December 13, 2023Medical DevicesFDA
Stryker Medical Division of Stryker Corporation recalls ProCuity bed series, model number 3009, item number: 300900000000,
Hazard: Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
July 19, 2023Medical DevicesFDA
Stryker Medical Division of Stryker Corporation recalls Power-PRO 2- A powered ambulance cot that consists of a platform, including a mattress, mounted on a wheeled, retractabl
Hazard: Base leg assembly may bend and result in difficulty engaging/disengaging from fastener, difficulty loading/unloading from ambulance, difficulty raising or lowering the cot, cot tip, or erratic or unintended motion.
March 22, 2023Medical DevicesFDA
Stryker Medical Division of Stryker Corporation recalls Power-PRO 2 . Intended as an ambulance cot to transport a patient to or from an emergency or non-emergency location. Mo
Hazard: Transport Cot has insufficient volume of epoxy to assemblies installed in the head section and foot sectioning system may result in separation of head end or foot end from the cot and result in unexpected disengagement while loading/unloading or transport.
December 21, 2022Medical DevicesFDA
Stryker Medical Division of Stryker Corporation recalls Power-PRO 2, Model No. 6507, Item No. 650705550001 (US); 650700000000 (International)
Hazard: Cot may experience unintended motion due to damaged cables. Potential risk of soft tissue injury to patients such as scrapes or bruises resulting from the cot lowering faster than expected.
August 18, 2021Medical DevicesFDA
Stryker Medical Division of Stryker Corporation recalls GoBed II MedSurg Bed, Model Number FL28, Part #FL28EX
Hazard: Medical devices intended for use in a healthcare facility were distributed to residential customers and may be in use in a home environment. The product s labeling accurately identifies the correct use environment, but home users may not be aware of or fully understand these instructions intended for healthcare professionals
August 18, 2021Medical DevicesFDA
Stryker Medical Division of Stryker Corporation recalls Electric MedSurg Bed FL23 - AC-powered adjustable hospital bed with four built-in electric DC motors and remote controls
Hazard: Medical devices intended for use in a healthcare facility were distributed to residential customers and may be in use in a home environment. The product s labeling accurately identifies the correct use environment, but home users may not be aware of or fully understand these instructions intended for healthcare professionals
August 18, 2021Medical DevicesFDA
Stryker Medical Division of Stryker Corporation recalls CUB Pediatric Crib- intended to provide a pediatric patient support surface for medical purposes and to provide a method
Hazard: Medical devices intended for use in a healthcare facility were distributed to residential customers and may be in use in a home environment. The product s labeling accurately identifies the correct use environment, but home users may not be aware of or fully understand these instructions intended for healthcare professionals
August 18, 2021Medical DevicesFDA
Stryker Medical Division of Stryker Corporation recalls Stretcher Chair-for use in all acute care hospitals and medical outpatient services Model Number: 5050¿¿¿¿ Part # 505
Hazard: Medical devices intended for use in a healthcare facility were distributed to residential customers and may be in use in a home environment. The product s labeling accurately identifies the correct use environment, but home users may not be aware of or fully understand these instructions intended for healthcare professionals
August 18, 2021Medical DevicesFDA
Stryker Medical Division of Stryker Corporation recalls Michael Graves with Stryker Highback Chair-intended for pediatric and adult person guest and patient seating use in an i
Hazard: Medical devices intended for use in a healthcare facility were distributed to residential customers and may be in use in a home environment. The product s labeling accurately identifies the correct use environment, but home users may not be aware of or fully understand these instructions intended for healthcare professionals
August 18, 2021Medical DevicesFDA
Stryker Medical Division of Stryker Corporation recalls Symmetry Plus Treatment Recliner - general hospital use as a convenient seating surface for patients or guests to sit, M
Hazard: Medical devices intended for use in a healthcare facility were distributed to residential customers and may be in use in a home environment. The product s labeling accurately identifies the correct use environment, but home users may not be aware of or fully understand these instructions intended for healthcare professionals
August 18, 2021Medical DevicesFDA
Stryker Medical Division of Stryker Corporation recalls TruRize Clinical Chair - support structure that places human occupants in upright, seated, recline, supine, and trend po
Hazard: Medical devices intended for use in a healthcare facility were distributed to residential customers and may be in use in a home environment. The product s labeling accurately identifies the correct use environment, but home users may not be aware of or fully understand these instructions intended for healthcare professionals
August 18, 2021Medical DevicesFDA
Stryker Medical Division of Stryker Corporation recalls S3 MedSurg Bed - intended to support and transport patients within the Med/Surg and Critical Care hospital environments,
Hazard: Medical devices intended for use in a healthcare facility were distributed to residential customers and may be in use in a home environment. The product s labeling accurately identifies the correct use environment, but home users may not be aware of or fully understand these instructions intended for healthcare professionals
August 18, 2021Medical DevicesFDA
Stryker Medical Division of Stryker Corporation recalls Isolibrium Support Surface - support surface assists in the prevention and treatment of all pressure injury stages (incl
Hazard: Medical devices intended for use in a healthcare facility were distributed to residential customers and may be in use in a home environment. The product s labeling accurately identifies the correct use environment, but home users may not be aware of or fully understand these instructions intended for healthcare professionals
August 18, 2021Medical DevicesFDA
Stryker Medical Division of Stryker Corporation recalls S3 MedSurg Bed - intended to support and transport patients within the Med/Surg and Critical Care hospital environments,
Hazard: Medical devices intended for use in a healthcare facility were distributed to residential customers and may be in use in a home environment. The product s labeling accurately identifies the correct use environment, but home users may not be aware of or fully understand these instructions intended for healthcare professionals
August 18, 2021Medical DevicesFDA
Stryker Medical Division of Stryker Corporation recalls IsoGel Air - support surface assists in the prevention and treatment of all pressure ulcers stages, Model Number 2860, P
Hazard: Medical devices intended for use in a healthcare facility were distributed to residential customers and may be in use in a home environment. The product s labeling accurately identifies the correct use environment, but home users may not be aware of or fully understand these instructions intended for healthcare professionals