Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit recall (Inter-Med Llc)
Medical deviceClass IIOngoing
Summary: Inter-Med Llc is recalling 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.
What is being recalled
Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28
Why
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.
How serious is it
Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
Where it was sold
US Nationwide distribution in the states of Tennessee and Missouri. (states named: Missouri, Tennessee)
How to tell if yours is affected
Model No. 504600-28; UDI-DI 00371347008104; Lot Number 2026-0204
What to do
Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.
Recall facts
| Recall number | Z-2400-2026 |
| Category | Medical device |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class II |
| Status | Ongoing |
| Recall started | May 27, 2026 |
| Reported | June 17, 2026 |
| Company | Inter-Med Llc |
| Company location | Racine, WI, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 500 |
More recalls from Inter-Med Llc · all medical device recalls · recalls from May 2026