Z-2400-2026 Class II Ongoing
FDA device recall Z-2400-2026 was initiated by Inter-Med Llc on May 27, 2026 and is designated Class II. 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 … The recall status is ongoing. Affected quantity: 500.
Recall Details
- Product Type
- Devices
- Report Date
- June 17, 2026
- Initiation Date
- May 27, 2026
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 500
Product Description
Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28
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 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.
Distribution Pattern
US Nationwide distribution in the states of Tennessee and Missouri.
Code Information
Model No. 504600-28; UDI-DI 00371347008104; Lot Number 2026-0204