Where can I verify this recall directly with FDA?

The verbatim FDA record is the source of truth for every recall Argus HQ tracks — always confirm against fda.gov before acting.

What should someone who has this product do?

Because this recall carries FDA's middle severity classification, anyone who has this product should stop using it and follow the recalling firm's instructions, even though serious harm is considered unlikely for this classification. Check the product against FDA's description (Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28) and recall number Z-2400-2026, then follow Inter-Med Llc's recall instructions.

FDA Class II Recall: Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit,… by Inter-Med Llc

Key facts

Recalling firm	Inter-Med Llc
Manufacturer	Not disclosed in the FDA record.
Brand name	Not disclosed in the FDA record.
Product description	Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28
Classification	Class II
Recall number	Z-2400-2026
Report date	Not disclosed in the FDA record.
Status	Ongoing
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.

The short version: Inter-Med Llc recalled Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28 on 2026-06-17. FDA classified this action as a Class II recall (recall number Z-2400-2026). 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 (additional items listed in FDA's full record). Recall status: Ongoing. This is a device-category FDA recall record.

What consumers should do

Because this recall carries FDA's middle severity classification, anyone who has this product should stop using it and follow the recalling firm's instructions, even though serious harm is considered unlikely for this classification. Specifically, check whether the product in your possession matches the description on file with FDA -- Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28 -- and the recall number Z-2400-2026. If it matches, stop using or distributing it and contact Inter-Med Llc or the point of purchase for return or replacement instructions. Retailers and distributors holding affected inventory should quarantine it and follow the firm's written recall notice. FDA maintains a public enforcement report database so that consumers, physicians, and purchasers can look up the exact product identifiers involved before deciding what to do.

What this classification means

FDA classifies a recall as Class II when using the recalled product, or being exposed to it, may cause temporary or medically reversible adverse health consequences, or when the probability of serious adverse health consequences is remote. In this case, the recalling firm is Inter-Med Llc and the affected product is described in FDA's record as: Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28. FDA's stated reason for the recall is: 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 (additional items listed in FDA's full record). The recall is tracked under FDA recall number Z-2400-2026 and carries a status of Ongoing as of the most recent FDA enforcement report. This classification reflects FDA's assessment of the product defect described above, not a prediction about any specific patient outcome. FDA maintains a public enforcement report database so that consumers, physicians, and purchasers can look up the exact product identifiers involved before deciding what to do. Recall status can change while FDA and the recalling firm continue corrective actions, so checking the firm's own notice for the most current guidance is recommended.

Inter-Med Llc’s FDA history

Argus HQ has recorded 1 total FDA action tied to Inter-Med Llc: 0 warning letters, 1 recall, 0 approval records, and 0 Form 483 inspection citations.

Frequently asked questions

Where can I verify this recall directly with FDA?: The verbatim FDA record is the source of truth for every recall Argus HQ tracks — always confirm against fda.gov before acting.
What was recalled and why?: Inter-Med Llc recalled Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28. FDA's record states the reason for recall as: 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 (additional items listed in FDA's full record). The recall is logged under FDA recall.
How serious is this recall?: FDA classifies a recall as Class II when using the recalled product, or being exposed to it, may cause temporary or medically reversible adverse health consequences, or when the probability of serious adverse health consequences is remote.
What should someone who has this product do?: Because this recall carries FDA's middle severity classification, anyone who has this product should stop using it and follow the recalling firm's instructions, even though serious harm is considered unlikely for this classification. Check the product against FDA's description (Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28) and recall number Z-2400-2026, then follow Inter-Med Llc's recall instructions.

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Full FDA history for Inter-Med Llc

Compiled by Argus HQ Research from FDA primary sources · Reviewed by Andy Gaber, Founder

Cite this record

Reusing this data in reporting or research? Here’s a ready-made citation.

APA

Argus HQ Research (2026). FDA Class II Recall: Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit,… by Inter-Med Llc. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/recall/fda-recall-inter-med-llc-z-2400-2026

MLA

"FDA Class II Recall: Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit,… by Inter-Med Llc." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/recall/fda-recall-inter-med-llc-z-2400-2026.

Chicago

Argus HQ Research. "FDA Class II Recall: Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit,… by Inter-Med Llc." Digital Empire Holdings LLC. Accessed August 13, 2026. https://argushq.ai/recall/fda-recall-inter-med-llc-z-2400-2026.

BibTeX

@misc{argushq_argushq_ai_recall_fda_recall_inter_med_llc_z_2400_2026_2026,
  title = {FDA Class II Recall: Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit,… by Inter-Med Llc},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/recall/fda-recall-inter-med-llc-z-2400-2026},
  note = {Accessed: August 13, 2026}
}

Source: FDA.gov — Recalls ↗