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All product recalls associated with Medtronic Sofamor Danek Instrument Manufacturing.
Total Recalls
39
Past Year
0
Class I (Serious)
0
Most Recent
Dec 2006
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.
Due to a manufacturing error, the proximal end may deform causing the protrusions that engage the associated implant to break off of the instrument during use.
Bone reamer may not have a cutting surface on the tip.
Due to a manufacturing error, after autoclaving, the Tubular Retractor coating, Physical Vapor Deposition (PVD) black Titanium Nitride (TiN), may rub off.