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All product recalls associated with Stryker Howmedica Osteonics Corp..
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.
Stryker was made aware that the short arm of the bone inserter may fracture during use and potentially result in an adverse health consequence.
The expiration date listed on the product label is greater than the vendor recommended expiration date.
The expiration date listed on the product label is greater than the vendor recommended expiration date.