Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit recall
Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28
Why was Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit recalled?
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 should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Model No. 504600-28; UDI-DI 00371347008104; Lot Number 2026-0204
- Product
- Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28
- Recalling firm
- Inter-Med Llc
- Quantity
- 500
- Distribution
- US Nationwide distribution in the states of Tennessee and Missouri.
- Recall date
- June 17, 2026
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)