Recall Z-2400-2026
Inter-Med Llc · initiated May 27, 2026
Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature
Product
Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28
Codes / lots: Model No. 504600-28; UDI-DI 00371347008104; Lot Number 2026-0204
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.
FDA-determined cause: Labeling mix-ups
Action taken
On 5/27/2026, firm notified consignees via email. Consignees were instructed to return all units from Lot 2026-0204 to Inter-Med, Inc. Inter-Med, Inc. will provide prepaid return shipping labels. All returned product will be replaced with correctly packaged product at no charge, or a credit may be issued at the customer's preference. Customers must also notify any downstream dental practices or end users who received product from this lot and instruct them to return product.
Details
- Recall number
- Z-2400-2026
- Initiated
- May 27, 2026
- Posted by FDA
- June 10, 2026
- Product code
- MVL – Cord, Retraction
- Quantity
- 500
- Distribution
- US Nationwide distribution in the states of Tennessee and Missouri.
- Recalling firm
- Inter-Med Llc, Racine, WI