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  "name": "UMARY ACID HYALURONIC, 850 MG CAPLETS, 30-count bottle, UPC7502265120323",
  "description": "FDA recall D-0166-2025 — MXBBB is recalling UMARY ACID HYALURONIC, 850 MG CAPLETS, 30-count bottle, UPC7502265120323 (Drugs, 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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  "dateModified": "2026-06-24T07:02:03.626072+00:00",
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      "name": "FDA recall D-0166-2025: MXBBB is recalling UMARY ACID HYALURONIC, 850 MG CAPLETS, 30-count bottle, UPC7502265120323",
      "text": "The FDA logged enforcement record D-0166-2025: MXBBB is voluntarily recalling UMARY ACID HYALURONIC, 850 MG CAPLETS, 30-count bottle, UPC7502265120323 — reason: cGMP Deviations: the firm initiated a recall after notification from the distributor that product may be tainted with undeclared diclofenac and omeprazole, however there is no analytical data confirming that product distributed by the firm is tainted.. Status: Ongoing — the recall is still being carried out.. Initiated 2024-11-14. Affected lots/codes: Lot#: 24183, Exp 07/01/28. A RECORDED FDA enforcement action (occurred=true).",
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      "name": "FDA classified recall D-0166-2025 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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      "falsifier": "occurred=FALSE (a framing, not an event) and adjudged=FALSE (an in-house reading, not an authority's verdict) — the LOWEST-warrant claim here. A flat representation would render this identically to the official facts; the four-status does not."
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            "Field": "Distribution pattern",
            "Value": "Product was sold via Amazon Marketplace.",
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