FDA Medical devices recall ·
Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit recall
- Recall number
- Z-2400-2026
- Date
- (initiated May 27, 2026)
- Company / brand
- Inter-Med Llc
2200 South St, Racine, WI, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 500
- Hazard tags
- Poisoning
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28
Why was it 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 you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Model No. 504600-28; UDI-DI 00371347008104; Lot Number 2026-0204
Distribution
US Nationwide distribution in the states of Tennessee and Missouri.
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-2400-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.