HIGHFDA DEVICE

Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28

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.

Inter-MedHealth & Personal CareMedical DevicesModel No. 504600-28UDI-DI 00371347008104Lot Number 2026-0204

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
May 27, 2026
Status
ACTIVE

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

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
  4. 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.

  1. Recall announced

    May 27, 2026

  2. Reported by FDA DEVICE

    June 17, 2026

  3. RecallRadar source check

    June 23, 2026

  4. 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.

Safety Guide

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Read: How to Get Refunds and Replacements

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Product Classification

Product Details

Model Numbers
Model No. 504600-28
UDI-DI 00371347008104
Lot Number 2026-0204
Affected States
ALL
Report Date
June 17, 2026
Recall Status
ACTIVE