- Recalling firm
- Inter-Med Llc
- 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.
- Affected products (lot / model / serial)
- Model No. 504600-28; UDI-DI 00371347008104; Lot Number 2026-0204
- Units affected
- 500
- Distribution pattern
- US Nationwide distribution in the states of Tennessee and Missouri.
- Firm location
- Racine, WI, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- N/A
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2400-2026
- Recall initiated
- May 27, 2026
- FDA classification date
- June 10, 2026
- FDA report date
- June 17, 2026
- FDA event ID
- 99105
- Last updated on HTM Vibe
- July 23, 2026