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All product recalls associated with Tornier S.A.S. 161 Rue Lavoisier Montbonnot St Martin France.
Total Recalls
2
Past Year
0
Class I (Serious)
0
Most Recent
Apr 2024
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.
Potential patient exposure to the graphite substrate.