Quick Facts at a Glance
- Recall Date
- May 27, 2026
- Hazard Level
- HIGH
- Brand
- Inter-Med
- Geographic Scope
- 1 states
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- Inter-Med
- Model numbers
- Model No. 504600-28, UDI-DI 00371347008104, Lot Number 2026-0204
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
May 27, 2026
Reported by FDA DEVICE
June 17, 2026
RecallRadar source check
June 23, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
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 You Should Do
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Inter-Med Llc or your healthcare provider for instructions. Notification method: N/A
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Full Description
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.. Classification: Class II. Quantity: 500. Distribution: US Nationwide distribution in the states of Tennessee and Missouri.
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Safety Guide
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