Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit — Class II medical device recall Z-2400-2026
Ongoing recall by Inter-Med Llc, reported 2026-06-17, distributed nationwide. Some units of Aluminum Chloride Gel contain the package insert for Ferric Sulfate Gel. The incorrect insert mi
| Recall number | Z-2400-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Inter-Med Llc, Racine, WI, United States |
| Recall initiated | 2026-05-27 |
| Classified | 2026-06-10 |
| Reported by FDA | 2026-06-17 |
| Distributed | Nationwide (US) |
| Quantity | 500 |
| UPC / GTIN / UDI-DI | 00371347008104 |
| Lot numbers | 2026-0204 |
| Model numbers | 504600-28 |
Product
Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2400-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.