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All product recalls associated with Depuy Orthopaedics, Inc..
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.
The ulnar bearing may damage the implant's polyethylene sleeve such that revision surgery is necessary.
Mislabeled boxes -- Scorpio PS Right Femoral Component No Posts contained a Scorpio PS Left Femoral Component with Posts and vice versa.
Dot matrix printer, as a component of a pressure monitoring system, may overheat and pose a fire hazard.