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All product recalls associated with Warsaw Orthopedic, Inc. dba Medtronic SOFAMOR DANEK.
Total Recalls
1000
Past Year
1000
Class I (Serious)
143
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 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.
GE Healthcare has received reports of breathing circuit or tubing misconnections of the Anesthesia Delivery Unit (ADU), that may impact patient safety.