Hemostatic Gel Kit Recall: Inter-Med Llc 504600-28
Announced 2026-06-17 · FDA
Some units of Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog 504600-28, contain the Ferric Sulfate Gel package insert by mistake. The incorrect insert misidentifies the product and contains different first aid instructions, including instructions to induce vomiting, whereas the correct Aluminum Chloride insert instructs not to induce vomiting. About 500 units were distributed in the US, including Tennessee and Missouri.
| Brand | 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. |
| Severity | moderate |
| Units affected | 500 |
| Distribution | US Nationwide distribution in the states of Tennessee and Missouri. |
| Agency | FDA |
| Recall / campaign no. | Model No. 504600-28; UDI-DI 00371347008104; Lot Number 2026-0204 |
WHAT YOU SHOULD DO
- Do not use the affected kit.
- Check if your unit is affected by verifying model 504600-28 and lot number 2026-0204.
- Contact Inter-Med Llc or the retailer for return, replacement, or disposal instructions.
- If you may have ingested the product, seek medical advice or contact poison control.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.