factually
Index/Topics/Class II Device Recalls

Class II Device Recalls

Class II recalls indicate potential for temporary or medically reversible adverse health consequences or a remote probability of serious adverse events according to FDA definitions.

Fact-Checks

1 result
Jan 27, 2026
Most Viewed

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, ...