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The recall of NeuroMax Cartridge by the FDA, including the manufacturer and corrective actions.
The has taken enforcement actions tied to products with names similar to "": the agency issued a warning letter to an entity marketing "" for unapproved COVID-related claims (NeuroXPF, 03/31/2020) and...
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, ...
The ’s public database lists a Class 2 recall for the “,” and that recall record is the primary public source for who manufactured the product and what corrective actions were announced . The reportin...