Class II — Inter-Med Llc
| Recalling firm | INTER-MED, INC. |
|---|---|
| Registered facility | View this company's 3 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Ongoing |
| 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. |
| Product | Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28 |
| Quantity | 500 |
| Distribution | US Nationwide distribution in the states of Tennessee and Missouri. |
| Initiated | 2026-05-27 |
| Classified | 2026-06-10 |
| Recall number | Z-2400-2026 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Inter-Med Llc (Z-2400-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/99105/
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