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All product recalls associated with Advanced Neuromodulation Systems.
Total Recalls
2
Past Year
0
Class I (Serious)
0
Most Recent
Jun 2009
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.
Product programmed with unapproved software was distributed.
Product's external charging system on occasion was failing to communicate with the Implantable Pulse Generator preventing re-charging of the pain relief system.