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All product recalls associated with Warsaw Orthopedic, Inc. dba Medtronic SOFAMOR DANEK.
Total Recalls
4
Past Year
0
Class I (Serious)
0
Most Recent
Oct 2008
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 thickness of the connector may be under specification, which could cause the implant to break during surgery or after implantation.
The thickness of the connector may be under specification, which could cause the implant to break during surgery or after implantation.
Assembly may be compromised: Two thread grooves are missing on the nut, which may cause damage to the bone screw and result in the need for the bone screw to be replaced.