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All product recalls associated with Tornier S.A.S. 161 Rue Lavoisier Montbonnot St Martin France.
Total Recalls
1000
Past Year
1000
Class I (Serious)
127
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 software bug allows for case planning with anatomic glenoid Perform / Perform Augmented implants and anatomic humeral Tornier Flex implant configurations that are incompatible and do not have regulatory approval.
Elevated levels of inorganic arsenic.
The firm identified that the measured patient leakage current in some devices significantly exceeded expected levels.