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  "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-2598-2024.jsonld",
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  "name": "PORTEX Bivona Tracheostomy Silicone Tube, labeled as:    a)\t4.0MM FLEXTEND PEDIATRIC PLUS STRAIGHT TRACH TUBE  , Product Code/List Number/Item Code 60PFPS40;   b)\t4.5MM FLEXTEND PEDIATRIC PLUS STRAIGHT TRACH TUBE  , Product Code/List Number/Item Code 60PFPS45;   c)\t5.0MM FLEXTEND PEDIATRIC PLUS STRAIGHT TRACH TUBE  , Product Code/List Number/Item Code 60PFPS50;   d)\t5.5MM FLEXTEND PEDIATRIC PLUS STRIAGHT TRACH TUBE , Product Code/List Number/Item Code 60PFPS55;   e)\t6.0MM FLEXTEND PEDIATRIC PLUS STRAIGHT TRACH TUBE  , Product Code/List Number/Item Code 60PFPS60",
  "description": "FDA recall Z-2598-2024 — Smiths Medical ASD Inc. is recalling PORTEX Bivona Tracheostomy Silicone Tube, labeled as:    a)\t4.0MM FLEXTEND PEDIATRIC PLUS STRAIGHT TRACH TUBE  , Product Code/List Number/Item Code 60PFPS40;   b)\t4.5MM FLEXTEND PEDIATRIC PLUS STRAIGHT TRACH TUBE  , Product Code/List Number/Item Code 60PFPS45;   c)\t5.0MM FLEXTEND PEDIATRIC PLUS STRAIGHT TRACH TUBE  , Product Code/List Number/Item Code 60PFPS50;   d)\t5.5MM FLEXTEND PEDIATRIC PLUS STRIAGHT TRACH TUBE , Product Code/List Number/Item Code 60PFPS55;   e)\t6.0MM FLEXTEND PEDIATRIC PLUS STRAIGHT TRACH TUBE  , Product Code/List Number/Item Code 60PFPS60 (Devices, Class I). 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": "openFDA drug & device enforcement (recall) reports",
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  "about": {
    "@type": "schema:MedicalDevice",
    "name": "PORTEX Bivona Tracheostomy Silicone Tube, labeled as:    a)\t4.0MM FLEXTEND PEDIATRIC PLUS STRAIGHT TRACH TUBE  , Product Code/List Number/Item Code 60PFPS40;   b)\t4.5MM FLEXTEND PEDIATRIC PLUS STRAIGHT TRACH TUBE  , Product Code/List Number/Item Code 60PFPS45;   c)\t5.0MM FLEXTEND PEDIATRIC PLUS STRAIGHT TRACH TUBE  , Product Code/List Number/Item Code 60PFPS50;   d)\t5.5MM FLEXTEND PEDIATRIC PLUS STRIAGHT TRACH TUBE , Product Code/List Number/Item Code 60PFPS55;   e)\t6.0MM FLEXTEND PEDIATRIC PLUS STRAIGHT TRACH TUBE  , Product Code/List Number/Item Code 60PFPS60",
    "manufacturer": {
      "@type": "schema:Organization",
      "name": "Smiths Medical ASD Inc."
    }
  },
  "claims": [
    {
      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-2598-2024/enforcement-record",
      "@type": "schema:Claim",
      "name": "FDA recall Z-2598-2024: Smiths Medical ASD Inc. is recalling PORTEX Bivona Tracheostomy Silicone Tube, labeled as:    a)\t4.0MM FLEXTEND PEDIATRIC PLUS STRAIGHT TRACH TUBE  , Product Code/List Number/Item Code 60PFPS40;   b)\t4.5MM FLEXTEND PEDIATRIC PLUS STRAIGHT TRACH TUBE  , Product Code/List Number/Item Code 60PFPS45;   c)\t5.0MM FLEXTEND PEDIATRIC PLUS STRAIGHT TRACH TUBE  , Product Code/List Number/Item Code 60PFPS50;   d)\t5.5MM FLEXTEND PEDIATRIC PLUS STRIAGHT TRACH TUBE , Product Code/List Number/Item Code 60PFPS55;   e)\t6.0MM FLEXTEND PEDIATRIC PLUS STRAIGHT TRACH TUBE  , Product Code/List Number/Item Code 60PFPS60",
      "text": "The FDA logged enforcement record Z-2598-2024: Smiths Medical ASD Inc. is voluntarily recalling PORTEX Bivona Tracheostomy Silicone Tube, labeled as:    a)\t4.0MM FLEXTEND PEDIATRIC PLUS STRAIGHT TRACH TUBE  , Product Code/List Number/Item Code 60PFPS40;   b)\t4.5MM FLEXTEND PEDIATRIC PLUS STRAIGHT TRACH TUBE  , Product Code/List Number/Item Code 60PFPS45;   c)\t5.0MM FLEXTEND PEDIATRIC PLUS STRAIGHT TRACH TUBE  , Product Code/List Number/Item Code 60PFPS50;   d)\t5.5MM FLEXTEND PEDIATRIC PLUS STRIAGHT TRACH TUBE , Product Code/List Number/Item Code 60PFPS55;   e)\t6.0MM FLEXTEND PEDIATRIC PLUS STRAIGHT TRACH TUBE  , Product Code/List Number/Item Code 60PFPS60 — reason: Smiths Medical has identified that the securement flange of specific lots of the Bivona Neonatal/Pediatric and Adult Tracheostomy products may tear because of a manufacturing defect.. Status: Ongoing — the recall is still being carried out.. Initiated 2024-05-29. Affected lots/codes: a) UDI/DI 15021312516838, Product Code/List Number/Item Code 60PFPS40, Lot Numbers:   3853451, 3853452, 3868260, 3877673, 3884242, 3894866, 3907983, 3917997, 3920962, 3920963, 3930049, 3930050, 3942548, 3942549, 3959326, 3959327, 3959328, 3991154, 4005645, 4005646, 4008216, 4015542, 4021422, 4029509, 4033723, 4035736, 4053709, 4056252, 4063182, 4077077, 4080799, 4086021, 4091400, 4093734, 4096847, 4110450, 4134035, 4138976, 4151008, 4153590, 4159979, 4159980, 4171546, 4180493, 4196275, 4206816, 4212777, 4221343, 4231496, 4237382, 4240148, 4254245, 4283238, 4331606, 4334998, 4334999, 4348464, 4348465, 4348466, 4358482, 4365800, 4365806, 4395783, 4399175;   b) UDI/DI 15021312516715, Product Code/List Number/Item Code 60PFPS45, Lot Numbers:  3868257, 3868258, 3877672, 3880693, 3891520, 3897886, 3904652, 3914574, 3926970, 3931142, 3942520, 3949033, 3955791, 3962587, 3982665, 3982666, 4008217, 4015541, 4035737, 4049432, 4063184, 4077109, 4086027, 4089291, 4093735, 4110451, 4125815, 4134023, 4151043, 4159947, 4161983, 4171547, 4179356, 4180469, 4196277, 4212778, 4223728, 4231497, 4237383, 4292165, 4331608, 4335000, 4348467, 4348470, 4357234, 4358484, 4383625, 4388165, 4389898, 4393407, 4395784, 4399176, 4400666;  c) UDI/DI 15021312516722, Product Code/List Number/Item Code 60PFPS50, Lot Numbers:  3853453, 3877645, 3884257, 3887719, 3887720, 3887721, 3911440, 3914569, 3918000, 3918001, 3920951, 3920952, 3952386, 3952387, 3962578, 3991155, 4005647, 4011378, 4023789, 4026678, 4035738, 4053714, 4066287, 4083930, 4091404, 4107568, 4113114, 4125823, 4131004, 4139006, 4148007, 4153594, 4161988, 4171548, 4196276, 4206817, 4231498, 4331609, 4335001, 4362851, 4362852, 4369595, 4393408, 4399177;  d) UDI/DI 15021312516739, Product Code/List Number/Item Code 60PFPS55, Lot Numbers:  3884265, 3887739, 3891524, 3897847, 3918016, 3923716, 3936570, 3946284, 3952336, 3952337, 3955798, 3991156, 4015543, 4026692, 4035739, 4053730, 4080794, 4097835, 4110452, 4128034, 4139022, 4151025, 4223729, 4237384, 4331612, 4335002, 4347206, 4358487, 4388166, 4399178;  e) UDI/DI 15021312516746, Product Code/List Number/Item Code 60PFPS60, Lot Numbers:  3874296, 3884264, 3891525, 3897850, 3907969, 3918009, 3920953, 3942510, 3942511, 3942512, 3949022, 3959307, 3959308, 3959309, 3982667, 4005648, 4015544, 4026681, 4035741, 4041958, 4053703, 4077088, 4091410, 4105253, 4107588, 4122424, 4134014, 4139016, 4145701, 4153605, 4168150, 4171549, 4180467, 4212779, 4217443, 4231500, 4240149, 4335003, 4345010, 4348471, 4374436, 4374437, 4399179, 4400667. A RECORDED FDA enforcement action (occurred=true).",
      "claimType": "official_fact",
      "reviewStatus": "current",
      "commercialInfluence": false,
      "epistemicStatus": {
        "occurred": true,
        "supported": true,
        "adjudged": true,
        "operative": true
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      "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-2598-2024&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-2598-2024&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."
    },
    {
      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-2598-2024/fda-classification",
      "@type": "schema:Claim",
      "name": "FDA classified recall Z-2598-2024 as Class I",
      "text": "The FDA assigned this recall Class I: Class I — the FDA judged there is a reasonable probability that use of the product would cause serious harm or death.. 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",
      "commercialInfluence": false,
      "epistemicStatus": {
        "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-2598-2024&lang=eng",
        "value": "Class I",
        "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-2598-2024&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-2598-2024/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,
        "operative": true
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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-2598-2024",
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          "item": {
            "Field": "Recall number",
            "Value": "Z-2598-2024",
            "Status": "recorded"
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          "position": 2,
          "item": {
            "Field": "Product type",
            "Value": "Devices",
            "Status": "recorded"
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          "position": 3,
          "item": {
            "Field": "Classification",
            "Value": "Class I",
            "Status": "determination"
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          "position": 4,
          "item": {
            "Field": "Status",
            "Value": "Ongoing — the recall is still being carried out.",
            "Status": "recorded"
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          "@type": "schema:ListItem",
          "position": 5,
          "item": {
            "Field": "Recalling firm",
            "Value": "Smiths Medical ASD Inc.",
            "Status": "recorded"
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          "position": 6,
          "item": {
            "Field": "Reason",
            "Value": "Smiths Medical has identified that the securement flange of specific lots of the Bivona Neonatal/Pediatric and Adult Tracheostomy products may tear because of a manufacturing defect.",
            "Status": "recorded"
          }
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          "item": {
            "Field": "Initiated",
            "Value": "2024-05-29",
            "Status": "recorded"
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          "position": 8,
          "item": {
            "Field": "Lot/code info",
            "Value": "a) UDI/DI 15021312516838, Product Code/List Number/Item Code 60PFPS40, Lot Numbers:   3853451, 3853452, 3868260, 3877673, 3884242, 3894866, 3907983, 3917997, 3920962, 3920963, 3930049, 3930050, 3942548, 3942549, 3959326, 3959327, 3959328, 3991154, 4005645, 4005646, 4008216, 4015542, 4021422, 4029509, 4033723, 4035736, 4053709, 4056252, 4063182, 4077077, 4080799, 4086021, 4091400, 4093734, 4096847, 4110450, 4134035, 4138976, 4151008, 4153590, 4159979, 4159980, 4171546, 4180493, 4196275, 4206816, 4212777, 4221343, 4231496, 4237382, 4240148, 4254245, 4283238, 4331606, 4334998, 4334999, 4348464, 4348465, 4348466, 4358482, 4365800, 4365806, 4395783, 4399175;   b) UDI/DI 15021312516715, Product Code/List Number/Item Code 60PFPS45, Lot Numbers:  3868257, 3868258, 3877672, 3880693, 3891520, 3897886, 3904652, 3914574, 3926970, 3931142, 3942520, 3949033, 3955791, 3962587, 3982665, 3982666, 4008217, 4015541, 4035737, 4049432, 4063184, 4077109, 4086027, 4089291, 4093735, 4110451, 4125815, 4134023, 4151043, 4159947, 4161983, 4171547, 4179356, 4180469, 4196277, 4212778, 4223728, 4231497, 4237383, 4292165, 4331608, 4335000, 4348467, 4348470, 4357234, 4358484, 4383625, 4388165, 4389898, 4393407, 4395784, 4399176, 4400666;  c) UDI/DI 15021312516722, Product Code/List Number/Item Code 60PFPS50, Lot Numbers:  3853453, 3877645, 3884257, 3887719, 3887720, 3887721, 3911440, 3914569, 3918000, 3918001, 3920951, 3920952, 3952386, 3952387, 3962578, 3991155, 4005647, 4011378, 4023789, 4026678, 4035738, 4053714, 4066287, 4083930, 4091404, 4107568, 4113114, 4125823, 4131004, 4139006, 4148007, 4153594, 4161988, 4171548, 4196276, 4206817, 4231498, 4331609, 4335001, 4362851, 4362852, 4369595, 4393408, 4399177;  d) UDI/DI 15021312516739, Product Code/List Number/Item Code 60PFPS55, Lot Numbers:  3884265, 3887739, 3891524, 3897847, 3918016, 3923716, 3936570, 3946284, 3952336, 3952337, 3955798, 3991156, 4015543, 4026692, 4035739, 4053730, 4080794, 4097835, 4110452, 4128034, 4139022, 4151025, 4223729, 4237384, 4331612, 4335002, 4347206, 4358487, 4388166, 4399178;  e) UDI/DI 15021312516746, Product Code/List Number/Item Code 60PFPS60, Lot Numbers:  3874296, 3884264, 3891525, 3897850, 3907969, 3918009, 3920953, 3942510, 3942511, 3942512, 3949022, 3959307, 3959308, 3959309, 3982667, 4005648, 4015544, 4026681, 4035741, 4041958, 4053703, 4077088, 4091410, 4105253, 4107588, 4122424, 4134014, 4139016, 4145701, 4153605, 4168150, 4171549, 4180467, 4212779, 4217443, 4231500, 4240149, 4335003, 4345010, 4348471, 4374436, 4374437, 4399179, 4400667",
            "Status": "recorded"
          }
        },
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          "position": 9,
          "item": {
            "Field": "Distribution pattern",
            "Value": "Worldwide distribution.",
            "Status": "recorded"
          }
        }
      ]
    }
  ]
}