FDA device enforcement
Cub Pediatric Crib, Model FL19H
Cribs sold in the USA are missing two access door warning labels.
Class IIReported ongoing
Distribution: US Nationwide distribution.
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Stryker Medical Division of Stryker Corporation recall records
19 reported ongoing
19 records in this archive. Latest source date Feb 18, 2026.
FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
Records and reported status
Official source for Cub Pediatric Crib, Model FL19H
FDA device enforcement
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 compa...
Class IIReported ongoing
Distribution: US, nationwide
FDA device enforcement
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 compa...
Class IIReported ongoing
Distribution: US, nationwide
FDA device enforcement
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.
Class IIReported ongoing
Distribution: Distribution US Nationwide including Puerto Rico, Australia, Canada, Chile, China, Mexico, Poland, Spain and Switzerland.
FDA device enforcement
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.
Class IIReported ongoing
Distribution: Distribution US Nationwide including Puerto Rico, Australia, Canada, Chile, China, Mexico, Poland, Spain and Switzerland.
FDA device enforcement
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.
Class IIReported ongoing
Distribution: Distribution US Nationwide including Puerto Rico, Australia, Canada, Chile, China, Mexico, Poland, Spain and Switzerland.
FDA device enforcement
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.
Class IIReported ongoing
Distribution: Distribution US Nationwide including Puerto Rico, Australia, Canada, Chile, China, Mexico, Poland, Spain and Switzerland.
FDA device enforcement
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.
Class IIReported ongoing
Distribution: Distribution US Nationwide including Puerto Rico, Australia, Canada, Chile, China, Mexico, Poland, Spain and Switzerland.
FDA device enforcement
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.
Class IIReported ongoing
Distribution: Distribution US Nationwide including Puerto Rico, Australia, Canada, Chile, China, Mexico, Poland, Spain and Switzerland.
FDA device enforcement
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.
Class IIReported ongoing
Distribution: Distribution US Nationwide including Puerto Rico, Australia, Canada, Chile, China, Mexico, Poland, Spain and Switzerland.
FDA device enforcement
ProCuity bed series, model number 3009, item number: 3009PX-Z-450.
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
Class IIReported ongoing
Distribution: Distribution US Nationwide including Puerto Rico, Australia, Canada, Chile, China, Mexico, Poland, Spain and Switzerland.
FDA device enforcement
ProCuity bed series, model number 3009, item number: 3009PX-ZM-450.
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
Class IIReported ongoing
Distribution: Distribution US Nationwide including Puerto Rico, Australia, Canada, Chile, China, Mexico, Poland, Spain and Switzerland.
FDA device enforcement
ProCuity bed series, model number 3009, item number: 3009PX-ZM-600.
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
Class IIReported ongoing
Distribution: Distribution US Nationwide including Puerto Rico, Australia, Canada, Chile, China, Mexico, Poland, Spain and Switzerland.
FDA device enforcement
ProCurity bed series, model number 3009, item number: 3009PX-ZMX-450.
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
Class IIReported ongoing
Distribution: Distribution US Nationwide including Puerto Rico, Australia, Canada, Chile, China, Mexico, Poland, Spain and Switzerland.
FDA device enforcement
ProCurity bed series, model number 3009, item number: 3009PX-ZMX-600.
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
Class IIReported ongoing
Distribution: Distribution US Nationwide including Puerto Rico, Australia, Canada, Chile, China, Mexico, Poland, Spain and Switzerland.
FDA device enforcement
ProCurity bed series, model number 3009, item number: 3009PX-ZX-450.
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
Class IIReported ongoing
Distribution: Distribution US Nationwide including Puerto Rico, Australia, Canada, Chile, China, Mexico, Poland, Spain and Switzerland.
FDA device enforcement
Power-PRO 2- A powered ambulance cot that consists of a platform, including a mattress, mounted on a wheeled, retractable X-frame that is designed to support and transport a max...
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.
Class IIReported ongoing
Distribution: Worldwide distribution - US Nationwide and the countries of Australia, Canada, Netherlands, Switzerland, United Kingdom.
FDA device enforcement
Power-PRO 2 . Intended as an ambulance cot to transport a patient to or from an emergency or non-emergency location. Model: 650705550001
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.
Class IIReported ongoing
Distribution: US Nationwide distribution in the states of NY, VA.
FDA device enforcement
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.
Class IIReported ongoing
Distribution: Worldwide Distribution: US (Nationwide) and Foreign to countries of: Australia, Canada, Netherlands, and United Kingdom.
Reasons in these listed records
- Cribs sold in the USA are missing two access door warning labels.
- 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 ar...
- Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
- 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.
These examples come from this result page and are not a ranking of every recall reason.
Checking Stryker Medical Division of Stryker Corporation
Is there a recall on stryker medical division of stryker corporation right now?
This archive contains 19 records, including 19 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product.
How do I check my package or product?
Compare the product, firm and lot, date, model or serial identifiers with the notice. Use the label-check guide if you need help locating an identifier.
Does a matching name mean every item is included?
A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall.
What if the search finds no matching record?
This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. Check source coverage and the agency's current notices.
Where can I find older records?
Use monthly archives or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page.