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  "name": "Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit,  Catalog number 504600-28",
  "description": "FDA recall Z-2400-2026 — Inter-Med Llc is recalling Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit,  Catalog number 504600-28 (Devices, Class II). The enforcement record is RECORDED; the classification is a DETERMINATION (FDA's regulatory verdict); the boundary is INTERPRETATION (a recall ≠ harm to a specific person). Source: openFDA. CC0.",
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      "name": "FDA recall Z-2400-2026: Inter-Med Llc is recalling Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit,  Catalog number 504600-28",
      "text": "The FDA logged enforcement record Z-2400-2026: Inter-Med Llc is voluntarily recalling 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.. Status: Ongoing — the recall is still being carried out.. Initiated 2026-05-27. Affected lots/codes: Model No. 504600-28; UDI-DI 00371347008104; Lot Number 2026-0204. A RECORDED FDA enforcement action (occurred=true).",
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      "name": "FDA classified recall Z-2400-2026 as Class II",
      "text": "The FDA assigned this recall Class II: Class II — the FDA judged the product may cause temporary or medically reversible harm, with a remote chance of serious harm.. This is the FDA's official risk classification — its regulatory DETERMINATION of the hazard category (a verdict constituted by the FDA's recognition, occurred=FALSE), adjudged=TRUE because the FDA issued it. It is NOT a measurement of harm to any specific person.",
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      "text": "A recall is a RECORDED FDA enforcement action — the FDA logged that a firm is removing or correcting a product, classed by the FDA's risk judgment. It does NOT establish that any specific unit is affected or caused harm; causation is not established. This record informs and compares — it is NOT medical advice and does not tell anyone to start or stop a drug or device. For a medical decision, route to the FDA recall record and a licensed pharmacist or prescriber.",
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            "Field": "Distribution pattern",
            "Value": "US Nationwide distribution in the states of Tennessee and Missouri.",
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