Drug recall
Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28
FDA recall event 99105 · Class II · Inter-Med Llc
Key facts
| Event ID | 99105 |
|---|---|
| Recall numbers | Z-2400-2026 |
| Recalling firm | Inter-Med Llc |
| Product type | Devices |
| Products | Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| 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… |
| Initiation date | May 27, 2026 |
| Report date | Jun 17, 2026 |
| City | Racine |
| State | WI |
| Country | United States |
| FEI number | 3000209941 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: