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  "name": "Brand Name: UNclog Eye Mask  Product Name: UNclog Eye Mask  Model/Catalog Number: AG23JW24 Serial # ag22  Product Description: Heated eye mask  Component: Heating unit, wire",
  "description": "FDA recall Z-2586-2024 — EYE COMFORT CARE LLC is recalling Brand Name: UNclog Eye Mask  Product Name: UNclog Eye Mask  Model/Catalog Number: AG23JW24 Serial # ag22  Product Description: Heated eye mask  Component: Heating unit, wire (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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  "dateModified": "2026-06-24T07:02:03.626072+00:00",
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      "name": "FDA recall Z-2586-2024: EYE COMFORT CARE LLC is recalling Brand Name: UNclog Eye Mask  Product Name: UNclog Eye Mask  Model/Catalog Number: AG23JW24 Serial # ag22  Product Description: Heated eye mask  Component: Heating unit, wire",
      "text": "The FDA logged enforcement record Z-2586-2024: EYE COMFORT CARE LLC is voluntarily recalling Brand Name: UNclog Eye Mask  Product Name: UNclog Eye Mask  Model/Catalog Number: AG23JW24 Serial # ag22  Product Description: Heated eye mask  Component: Heating unit, wire — reason: Due to a change in the safety clips for the heated eye masks, the wires to the safety clips may detach as a result of tugging and pulling and may cause a short in the heating element of the mask and could potentially cause burn injuries.. Status: Completed — the FDA has determined all recalling-firm actions are complete (the FDA's review may still be open).. Initiated 2024-02-08. Affected lots/codes: Lot Code: AG23JW24 Serial # ag22. A RECORDED FDA enforcement action (occurred=true).",
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      "name": "FDA classified recall Z-2586-2024 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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      "@type": "schema:Claim",
      "name": "What an FDA recall is — and is NOT",
      "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": "Reason",
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