Inter-Med recalls Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit (Catalog 504600-28) due to incorrect package insert that may instruct users to induce vomiting after ingestion, which is unsafe. Affected units contain Ferric Sulfate Gel instructions instead of proper Aluminum Chloride instructions.
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.
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Contact the company
📍Recalling firmInter-Med Llc2200 South St · Racine, WI 53404-1510
✎ GovInfoNow plain-language explainer
Inter-Med is recalling some Advance Aluminum Chloride Gel Clear Hemostatic Gel Kits because they include the wrong package insert for Ferric Sulfate Gel. This insert incorrectly advises inducing vomiting after ingestion, which could cause harm. The correct insert says not to induce vomiting. Consumers should check their kit's catalog number and contact Inter-Med for details. Read more at govinfonow.com/recall/49069-inter-med-advance-aluminum-chloride-gel-kit-recall-incorrect-package.
“Inter-Med Advance Aluminum Chloride Gel Kit Recall: Incorrect Package Insert Risks.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/49069-inter-med-advance-aluminum-chloride-gel-kit-recall-incorrect-package. Based on FDA recall #Z-2400-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2400-2026%22&limit=1).
The FDA announced on May 27, 2026, that Inter-Med Llc is recalling the Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit due to a labeling error. Some units contain an incorrect package insert for Ferric Sulfate Gel, which provides dangerous first aid instructions. Owners should stop using the product and contact the company for a replacement.
How to tell if you have it
Brand: Inter-Med
Product: Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit
Catalog number: 504600-28
Model No.: 504600-28
UDI-DI: 00371347008104
Lot Number: 2026-0204
Distribution: Tennessee and Missouri
The hazard
The hazard involves some units containing the package insert for Ferric Sulfate Gel instead of the correct Aluminum Chloride insert. This misidentification is critical because the incorrect insert instructs users to induce vomiting if ingested, whereas the correct instructions advise against inducing vomiting.
Context
GovInfoNow's records show Inter-Med Llc has one other recall on record since June 27, 2019. That earlier recall involved Vista Dental Bleach Syringes with degrading bungs. Other recent recalls of similar products include the Avanos Medical PEG Kit 20 Fr PUSH OTW Recall (April 30, 2026) and the Medline Convenience Kits Recall (July 10, 2026).
How to tell if you have this one
Check the catalog number on the product, which is 504600-28. The kit may have a package insert labeled for Ferric Sulfate Gel instead of Aluminum Chloride Gel.
Brand
Inter-Med
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Details
Verify the catalog number (504600-28) and look for the Ferric Sulfate Gel package insert.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 2 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “US Nationwide distribution in the states of Tennessee and Missouri.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Missouri, Tennessee.
Recall timeline
FDA published this recall 21 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-2400-2026 (May 27, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2400-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.