Inter-med Llc: Cord, Retraction
Recall Summary Inter-Med LLC is recalling Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit (catalog number 504600-28) because some units contain the wrong instruction manual—the insert for Ferric Sulfate Gel instead of Aluminum Chloride Gel. The incorrect instructions give different first aid guidance for accidental ingestion, specifically telling users to induce vomiting when the correct instructions say not to. The affected product was distributed nationwide.
- Recalling firm
- Inter-Med Llc
- Product
- 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.
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-05-27
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- US Nationwide distribution in the states of Tennessee and Missouri.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/b44486cf-de90-4482-8a7a-6e263fa3b5aa