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  "name": "Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System",
  "description": "FDA recall Z-2282-2026 — Stryker Corporation is recalling Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System (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-2282-2026: Stryker Corporation is recalling Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System",
      "text": "The FDA logged enforcement record Z-2282-2026: Stryker Corporation is voluntarily recalling Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System — reason: It has been identified that the impacted docking station (SN 2521008873) was not product released from manufacturing and may not have completed required testing prior to being shipped to your facility. There is a potential risk of electrical shock due to the device s safety testing being unverifiable.. Status: Ongoing — the recall is still being carried out.. Initiated 2026-05-06. Affected lots/codes: GTIN 07613327634914, Serial Number 2521008873. A RECORDED FDA enforcement action (occurred=true).",
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      "name": "FDA classified recall Z-2282-2026 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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      "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": "US Nationwide distribution in the state of Indiana.",
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