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All product recalls associated with Medtronic Neurosurgery.
Total Recalls
1000
Past Year
426
Class I (Serious)
54
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.
Dura regeneration matrix may have out-of-specification endotoxin levels due to issues with in-process and finished goods endotoxin testing, which may present clinically with signs and symptoms of an acute inflammatory process, comparable to infection.
Draeger has become aware of instances where the device stopped working when in use when transitioning from battery to AC operation.
Undeclared Milk