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All product recalls associated with Stryker Instruments Div. of Stryker Corporation.
Total Recalls
1000
Past Year
731
Class I (Serious)
175
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.
A component of the device is a Dell laptop computer, which contains batteries that are under recall because they can overheat and cause a fire.
DESIGN FLAW: Issues were reported concerning fracture of handle, difficulty in removing inserter and inserter difficult to lock.
Reports of failure of the Luer Lok Access Device to lock securely to certain catheter devices because the male luer taper surface is not within the specification.