FDA Medical Device · Z-2400-2026

Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28

Class II · Ongoing

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.

Affected lots / codes — check yours against thisModel No. 504600-28; UDI-DI 00371347008104; Lot Number 2026-0204

Recalling firm: Inter-Med Llc, Racine, WI
Classification: Class II (temporary or reversible harm possible)
Status: Ongoing
Quantity: 500
Distribution: US Nationwide distribution in the states of Tennessee and Missouri.
Recall initiated: May 27, 2026
Classified: June 10, 2026
Initiation: Voluntary: Firm initiated

Official source. This record is published by the U.S. FDA through the openFDA enforcement database. View the unmodified government record:
https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2400-2026%22

Important. Recalls target specific lots and codes — compare the affected lots above against your own product. This page reproduces public FDA data for readability; EveryRecall is independent and not affiliated with the FDA.

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