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Medical Device Recalls Database

The FDA’s Medical Device Recalls database contains an entry titled Class 2 Device Recall NeuroMax Cartridge, confirming a classified action is recorded in the agency’s system.

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Jan 27, 2026
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What are the full details and dates of the FDA Class II recall for the NeuroMax Cartridge?

The has a recorded device recall entry for the "" in its medical device recall database (accessdata.fda.gov), but the publicly provided search snippets do not include the recall narrative, firm name, ...