Inter-Med Llc recalls Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit
- Recalling company
- Inter-Med Llc
- Product
- Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28
- Reason
- 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.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- May 27, 2026
- Reported
- Jun 17, 2026
- Distribution
- US Nationwide distribution in the states of Tennessee and Missouri.
- Status
- Ongoing
- Quantity
- 500
- Lot / codes
- Model No. 504600-28; UDI-DI 00371347008104; Lot Number 2026-0204
- Company location
- Racine, WI
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2400-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2400-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.