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  "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-2261-2026.jsonld",
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  "name": "COVIDIEN Shiley Tracheostomy Tube Cuffed with Inner Cannula REF 6FEN  UDI-DI code: 60884522007028    The devices are intended for use in providing tracheal access for airway management.  Shiley Tracheostomy Tubes are double cannula tracheostomy tubes with reusable  inner cannulae (LPC, FEN, CFS, CFN, LGT) and twist-lock connectors. These Shiley  Tracheostomy Tubes have a radiopaque, biocompatible outer cannula constructed of  polyvinyl chloride.",
  "description": "FDA recall Z-2261-2026 — Covidien LLC is recalling COVIDIEN Shiley Tracheostomy Tube Cuffed with Inner Cannula REF 6FEN  UDI-DI code: 60884522007028    The devices are intended for use in providing tracheal access for airway management.  Shiley Tracheostomy Tubes are double cannula tracheostomy tubes with reusable  inner cannulae (LPC, FEN, CFS, CFN, LGT) and twist-lock connectors. These Shiley  Tracheostomy Tubes have a radiopaque, biocompatible outer cannula constructed of  polyvinyl chloride. (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.",
  "license": "https://creativecommons.org/publicdomain/zero/1.0/",
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  "dateModified": "2026-06-24T07:02:03.626072+00:00",
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    "@type": "schema:Dataset",
    "name": "openFDA drug & device enforcement (recall) reports",
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  "sameAs": "https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=Z-2261-2026&lang=eng",
  "about": {
    "@type": "schema:MedicalDevice",
    "name": "COVIDIEN Shiley Tracheostomy Tube Cuffed with Inner Cannula REF 6FEN  UDI-DI code: 60884522007028    The devices are intended for use in providing tracheal access for airway management.  Shiley Tracheostomy Tubes are double cannula tracheostomy tubes with reusable  inner cannulae (LPC, FEN, CFS, CFN, LGT) and twist-lock connectors. These Shiley  Tracheostomy Tubes have a radiopaque, biocompatible outer cannula constructed of  polyvinyl chloride.",
    "manufacturer": {
      "@type": "schema:Organization",
      "name": "Covidien LLC"
    }
  },
  "claims": [
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      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-2261-2026/enforcement-record",
      "@type": "schema:Claim",
      "name": "FDA recall Z-2261-2026: Covidien LLC is recalling COVIDIEN Shiley Tracheostomy Tube Cuffed with Inner Cannula REF 6FEN  UDI-DI code: 60884522007028    The devices are intended for use in providing tracheal access for airway management.  Shiley Tracheostomy Tubes are double cannula tracheostomy tubes with reusable  inner cannulae (LPC, FEN, CFS, CFN, LGT) and twist-lock connectors. These Shiley  Tracheostomy Tubes have a radiopaque, biocompatible outer cannula constructed of  polyvinyl chloride.",
      "text": "The FDA logged enforcement record Z-2261-2026: Covidien LLC is voluntarily recalling COVIDIEN Shiley Tracheostomy Tube Cuffed with Inner Cannula REF 6FEN  UDI-DI code: 60884522007028    The devices are intended for use in providing tracheal access for airway management.  Shiley Tracheostomy Tubes are double cannula tracheostomy tubes with reusable  inner cannulae (LPC, FEN, CFS, CFN, LGT) and twist-lock connectors. These Shiley  Tracheostomy Tubes have a radiopaque, biocompatible outer cannula constructed of  polyvinyl chloride. — reason: Due to customer complaint regarding incorrect display box labeling.. Status: Ongoing — the recall is still being carried out.. Initiated 2026-04-15. Affected lots/codes: Product Number: 6FEN UDI-DI code: 60884522007028 Lot Number: 25H0868JZX. A RECORDED FDA enforcement action (occurred=true).",
      "claimType": "official_fact",
      "reviewStatus": "current",
      "commercialInfluence": false,
      "epistemicStatus": {
        "occurred": true,
        "supported": true,
        "adjudged": true,
        "operative": true
      },
      "grounding": {
        "groundingType": "SourceCitation",
        "source": "openFDA drug & device enforcement (recall) reports — U.S. FDA",
        "sourceUrl": "https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=Z-2261-2026&lang=eng",
        "value": "Devices recall, status Ongoing",
        "adjudicator": {
          "name": "openFDA drug & device enforcement (recall) reports — U.S. FDA",
          "url": "https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=Z-2261-2026&lang=eng"
        }
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      "falsifier": "A RECORD of measured/reported events (occurred=true) from openFDA drug & device enforcement (recall) reports — U.S. FDA; superseded when openFDA drug & device enforcement (recall) reports — U.S. FDA publishes its next release."
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      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-2261-2026/fda-classification",
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      "name": "FDA classified recall Z-2261-2026 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.",
      "claimType": "regulatory_determination",
      "reviewStatus": "current",
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        "occurred": false,
        "supported": true,
        "adjudged": true,
        "operative": true
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      "grounding": {
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        "source": "U.S. FDA recall classification (openFDA enforcement)",
        "sourceUrl": "https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=Z-2261-2026&lang=eng",
        "value": "Class II",
        "adjudicator": {
          "name": "U.S. FDA recall classification (openFDA enforcement)",
          "url": "https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=Z-2261-2026&lang=eng"
        }
      },
      "falsifier": "occurred=FALSE: a regulatory DETERMINATION (an authority's classification/judgment) has NO material truthmaker independent of recognition — it is constituted by U.S. FDA recall classification (openFDA enforcement)'s say-so (a Searle institutional fact), not measured. adjudged=TRUE because U.S. FDA recall classification (openFDA enforcement) (an external authority) issued it. Distinct from a recorded measurement (which has an independent truthmaker) and from a modeled figure (a computed quantity, not a verdict). Challengeable; superseded if the authority reclassifies."
    },
    {
      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-2261-2026/boundary",
      "@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.",
      "claimType": "interpretation",
      "reviewStatus": "current",
      "commercialInfluence": false,
      "epistemicStatus": {
        "occurred": false,
        "supported": true,
        "adjudged": false,
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      "grounding": {
        "groundingType": "Interpretation",
        "source": "Atlas Commons L5 boundary (enforcement-action ≠ harm causation)",
        "sourceUrl": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/",
        "value": "a recorded enforcement action, not proof of harm or causation; not medical advice",
        "adjudicator": null
      },
      "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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      "name": "FDA recall details — Z-2261-2026",
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            "Value": "Z-2261-2026",
            "Status": "recorded"
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            "Value": "Devices",
            "Status": "recorded"
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            "Field": "Classification",
            "Value": "Class II",
            "Status": "determination"
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          "item": {
            "Field": "Status",
            "Value": "Ongoing — the recall is still being carried out.",
            "Status": "recorded"
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          "position": 5,
          "item": {
            "Field": "Recalling firm",
            "Value": "Covidien LLC",
            "Status": "recorded"
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          "item": {
            "Field": "Reason",
            "Value": "Due to customer complaint regarding incorrect display box labeling.",
            "Status": "recorded"
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            "Field": "Initiated",
            "Value": "2026-04-15",
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            "Value": "Product Number: 6FEN UDI-DI code: 60884522007028 Lot Number: 25H0868JZX",
            "Status": "recorded"
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          "item": {
            "Field": "Distribution pattern",
            "Value": "Worldwide - U.S.: Nationwide distribution in the state of TX and the countries of France, French, Polynesia, Italy, Pakistan, Poland, Portugal, Spain, and Taiwan.",
            "Status": "recorded"
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