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All product recalls associated with Medtronic Sofamor Danek USA Inc.
Total Recalls
275
Past Year
5
Class I (Serious)
17
Most Recent
Dec 2025
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.
Engraving on implants may not match what is listed on the pouch labels.
Discovered swollen cans
Standard packed within NEFA kit has been assigned incorrectly. Calibrating with the incorrect value will cause a positive shift of up to +8% with both quality controls and patient samples