{"url_path":"/fda/device/recalls/Z-2400-2026","section_key":"summary","section_title":"DEVICE Recall: Inter-Med Llc — Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit,  Catalog number 504600-28","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-05-27","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2400-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Inter-Med Llc"},"word_count":117,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2400-2026\n\n**Recalling firm:** Inter-Med Llc\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-05-27\n**Report date:** 2026-06-17\n\n## Product\nAdvance Aluminum Chloride Gel Clear Hemostatic Gel Kit,  Catalog number 504600-28\n\n## Reason\nSome 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.\n\n## Affected lots\nModel No. 504600-28; UDI-DI 00371347008104; Lot Number 2026-0204\n\n## Distribution\nUS Nationwide distribution in the states of Tennessee and Missouri."}