Stryker Medical Division of Stryker recalls
6 official recalls and safety alerts involving Stryker Medical Division of Stryker since 2022-12, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.
This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with Stryker Medical Division of Stryker or the relevant agency.
- 2026-03-25
USStryker Medical Division of Stryker Corporation recalls Cub Pediatric Crib, Model FL19H
Cribs sold in the USA are missing two access door warning labels.
FDA · DeviceStryker Medical Division of Stryker CorporationUS Nationwide distribution.Official notice →- 2025-12-17
- US
Stryker Medical Division of Stryker Corporation recalls 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…
- 2023-12-13
- US
Stryker Medical Division of Stryker Corporation recalls 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.
FDA · DeviceStryker Medical Division of Stryker CorporationDistribution US Nationwide including Puerto Rico, Australia, Canada, Chile,…Official notice → - 2023-07-19
- US
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,…
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.
FDA · DeviceStryker Medical Division of Stryker CorporationWorldwide distribution - US Nationwide and the countries of Australia, Canada,…Official notice → - 2023-03-22
- US
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…
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…
FDA · DeviceStryker Medical Division of Stryker CorporationUS Nationwide distribution in the states of NY, VA.Official notice → - 2022-12-21
- US
Stryker Medical Division of Stryker Corporation recalls Power-PRO 2, Model No. 6507, Item No. 650705550001 (US); 650700000000 (International)
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.
FDA · DeviceStryker Medical Division of Stryker CorporationWorldwide Distribution: US (Nationwide) and Foreign to countries of:…Official notice →