Class II

Medical Device Recall: Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28

Inter-Med Llc · May 27, 2026

Reason for Recall

Some units of Aluminum Chloride Gel contain the package insert for Ferric Sulfate Gel. The incorrect insert misidentifies the product and contains different first aid instructions, most critically in that the Ferric Sulfate insert instructs users to induce vomiting in the case of ingestion, while the correct Aluminum Chloride insert instructs users not to induce vomiting.

Distribution

US Nationwide distribution in the states of Tennessee and Missouri.

States Affected

NATIONWIDE

Quantity Affected

500

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2400-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Inter-Med Llc Medical Device Recall: Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28 | SafeCheck