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All product recalls associated with Stryker Medical Div. of Stryker Corporation.
Total Recalls
1000
Past Year
1000
Class I (Serious)
34
Most Recent
Jan 2026
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
The head section backrest (fowler) may not raise up, or, if up, may drop suddenly due to wearing out of the actuator threads on the fowler.
Product malfunction-- hub may leak at connection to the shaft due to insufficient adhesive curing.
Hydrophilic guidewires have the potential to demonstrate degradation of the Pebax cladding.