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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.
Assembly problems: MIS instruments (Triathlon MIS AP Sizer Body - Left; Triathlon MIS Sizer Body - Right; Triathlon MIS Femoral Adjustment Block and Triathlon MIS Modular Capture) may not assemble properly.
The recalled steering shafts were installed on the following models: All 2002 440 Sno Pro Models All 2003 Firecat 500/600/700, Firecat 700 Sno Pro, and 440 Sno Pro Models All 2004 Firecat 500/600/700 (STD and Sno Pro), and Sabercat 500/600/700 Models All 2005 Firecat 500/600/700 (STD and Sno Pro), M5,M6,M7, and Sabercat 500/600/700 Models All 2006 Crossfire 600/700, Firecat 500/600/700, Firecat 700 Sno Pro, Sabercat 500/600/700, and all M-Series
Due to a potential sterility issue with the product container. Three lots sold in Japan were found to have bacterial contamination, which compromised sterility. Because of this production-line issue at the firm''s plant in China, AMO is recalling lots that were manufactured on the same production lines during the same production period.