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All product recalls associated with Medtronic Neuromodulation.
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.
Disconnection of the Medtronic sutureless connector (SC) catheters from the catheter port on the pump, or occlusion between the sutureless pump connector and the catheter port on the pump.
Monitor ceiling carriage may separate from the monitor ceiling suspension.
Due to an improper fixture revision, device may be missing a screw at the jaw assembly, resulting in jaw components falling off during use.