Every recall we track for Stryker Medical Division of Stryker Corporation — 51 in all — plus the complaints and injury reports the public filed about them.
Stryker recalls Cub Pediatric Crib Model FL19H in the USA for missing two access door warning labels. This could lead to safety risks if the labels are needed for proper use.
Stryker recalls certain MV3 bariatric beds and Arise 1000EX mattresses sold together without compatibility testing. These products are not designed to be used together and may cause issues.
Stryker recalls certain Arise 1000EX mattresses (Part Number 2236000000) sold near MV3 beds due to untested compatibility. These products are not designed to be used together.
Stryker recalls ProCuity bed model 3009 with missing electrical safety test values, risking tissue burn or shock. Affected units have specific serial numbers and item numbers.
Stryker recalls ProCuity bed series model 3009 with missing electrical safety test values, risking tissue burn or electrical shock. Affected units have specific serial numbers listed.
Stryker recalls ProCuity bed model 3009 (item 3009PX-ZM-600) due to missing electrical safety test values that could cause tissue burns or electrical shock. Affected units have specific serial numbers and UDI-DI codes.
Stryker recalls ProCuity bed model 3009 with missing electrical safety test values, risking tissue burn or electrical shock. Affected units have specific serial numbers and item numbers.
Stryker recalls ProCuity bed model 3009 with missing electrical safety test values, risking tissue burn or electrical shock during use.
Stryker recalls ProCurity bed model 3009 with missing electrical safety test values, risking tissue burns or electrical shock during use.
Stryker recalls ProCuity bed model 3009 with missing electrical safety tests, risking tissue burns or shock. Affected units have specific serial numbers and item numbers.
Stryker recalls ProCurity bed model 3009 (item number 3009PX-ZX-450) due to missing electrical safety test values, which could cause tissue burns or electrical shock. Affected units have specific serial numbers and UDI-DI codes.
Stryker recalls ProCuity bed model 3009 with missing electrical safety test values, risking tissue burn or electrical shock. Affected units have specific serial numbers and item numbers.
Stryker recalls ProCurity bed model 3009 with missing electrical safety test values that could cause electrical shock or tissue burns. Affected units have specific serial numbers and item numbers.
Stryker recalls ProCuity bed model 3009 with missing electrical safety tests that could cause tissue burns or electrical shock. Affected units have specific serial numbers and item numbers.
Stryker recalls ProCuity bed model 3009 with missing electrical safety tests that could cause tissue burns or electrical shock. Affected units have specific serial numbers and item numbers.
Stryker recalls ProCuity bed model 3009 with missing electrical safety test values, risking tissue burns or electrical shock. Affected units have specific serial numbers and item numbers.
Stryker recalls Power-PRO 2 ambulance cots with serial numbers from 2112001485 to 2211001651. The base leg assembly may bend, causing difficulty engaging/disengaging from fasteners and affecting loading/unloading from ambulances. Affected units shipped between February 2022 and February 2023.
Stryker recalls Power-PRO 2 ambulance cots with insufficient epoxy causing head or foot sections to detach during transport. Affected units have specific serial numbers. Contact Stryker for repair or replacement.
Stryker recalls Power-PRO 2 cots with model 6507 that may move unexpectedly due to damaged cables, risking soft tissue injuries like scrapes or bruises to patients.
Stryker recalls Prime TC transport chairs sold to homes, which were intended for healthcare facilities. Home users may not follow proper safety instructions for medical use.
Stryker recalls Isolibrium Support Surfaces sold to homes. These medical-grade products are intended for healthcare facilities only. Home users may not understand proper use, risking pressure injuries.
Stryker recalls TruRize Clinical Chairs sold to homes. These medical chairs are designed for healthcare facilities but may be used at home without proper understanding of safety instructions.
Stryker recalls FL23 hospital beds sold to homes due to improper use instructions. Home users may not understand healthcare-specific safety requirements.
Stryker recalls Surgistool Model 830 for home use. Healthcare devices distributed to residential customers may cause injury if used incorrectly without professional training.
Stryker recalls IsoGel Air support surfaces (Model 2860) sold to homes. These medical devices are intended for healthcare facilities only; home users may not follow proper instructions.
Stryker recalls GoBed II MedSurg Beds (model FL28) sold to homes. These hospital-grade beds may cause injury if used outside healthcare settings without proper training.
Stryker recalls Symmetry Plus Treatment Recliners sold to homes. These hospital-grade chairs may cause injury if used incorrectly in residential settings due to unmet safety requirements.
Stryker recalls ComfortGel model 2850 for home use without healthcare professional guidance, risking improper pressure injury treatment.
Stryker recalls hospital-grade stretcher chairs sold to homes due to incorrect use environment labeling. Home users may not follow healthcare-specific instructions, risking injury.
Stryker recalls CUB Pediatric Crib devices sold to homes, which were intended for healthcare facilities. Home users may not understand proper use, risking injury.
Stryker recalls Transport Stretcher 747 for home use without healthcare training. This medical device may cause injury if misused in residential settings where professional instructions are not followed.
Stryker recalls S3 MedSurg Beds sold to homes, which are designed for hospitals. Home users may not follow healthcare instructions, risking injury.
Stryker recalls InTouch 2131 medical device sold to homes instead of hospitals. Home users may not understand healthcare-specific instructions, risking improper use.
Stryker recalls Michael Graves Highback Chairs (Model 4853) sold to homes. These chairs are designed for healthcare facilities but may be used at home without proper understanding of safety instructions.
Stryker recalls S3 MedSurg Beds sold to homes, which are designed for hospitals. Home users may not follow healthcare instructions, risking injury.
Stryker recalls Prime Big Wheel Stretcher (Model 1115) for home use. Healthcare devices distributed to residential customers may cause injury if misused without professional training.
Stryker recalls Proform support surfaces sold to homes for pressure ulcer care. Home users may not follow healthcare instructions, risking injury. Contact Stryker for details.
Stryker recalls Prime Fifth Wheel Stretcher model 1105 for home use. The device is intended for healthcare facilities but may be used at home without proper training, risking injury.
Stryker recalls IsoAir 2.0 support surfaces with potential CPR connector removal issues during cardiac arrest. Affected units have specific serial numbers and model 2941-001-100. Contact Stryker for details.
Stryker recalls Power-PRO TL ambulance cots (model 6550) that may not meet crash test standard BS EN 1789. Affected units include specific serial numbers listed in the recall notice.
Stryker recalls Power-LOAD Cot Fastening System Model 6390 (Catalog #6390-000-000) due to risk of broken floor plates during ambulance patient transport. Affected units have serial numbers listed in the recall notice.
Stryker is a global leader in medical technology, providing innovative solutions for healthcare professionals and patients worldwide.
Stryker recalls Spirit Select Bed Model 5700 Spirit Plus with high rail siderail option due to potential entrapment risk. Affected units have specific serial numbers listed in the recall notice.
Stryker recalls Spirit Plus Bed Model 5600 with high rail siderail option due to potential entrapment risk. Affected units have specific serial numbers listed in the recall notice.
Stryker recalls Altrix Model 8001 units made between Oct 2016 and June 2017 due to potential alarm fatigue and device faults that could affect patient temperature monitoring.
Stryker recalls 2860 IsoFlex LAL Support Surfaces with non-conforming fire barrier. These medical devices for pressure injury prevention may pose fire risk if improperly used in healthcare settings.
Stryker recalls specific 6376 M-1 Cot Fasteners with missing safety warnings in manuals. Owners should check serial numbers and contact Stryker for details.
Stryker recalls 6381 M-1 Cot Fasteners with missing safety warnings in manuals. Owners should check serial numbers 170740538-170740540 for affected units.
Stryker recalls T/Pump temperature therapy pumps (models TP700 and TP700C) due to incorrect manual updates adding 'heat conservation for normothermia maintenance' to indications. No immediate action needed as the hazard is a documentation error.
