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  "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-0888-2025.jsonld",
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  "name": "GE Healthcare Infinia I, Model/Catalog Numbers:    1) 5178728,   2) H3000WE,   3) H3000WM,   4) H3000YG; System, Tomography, Computed, Emission",
  "description": "FDA recall Z-0888-2025 — GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING is recalling GE Healthcare Infinia I, Model/Catalog Numbers:    1) 5178728,   2) H3000WE,   3) H3000WM,   4) H3000YG; System, Tomography, Computed, Emission (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": "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-0888-2025&lang=eng",
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    "@type": "schema:MedicalDevice",
    "name": "GE Healthcare Infinia I, Model/Catalog Numbers:    1) 5178728,   2) H3000WE,   3) H3000WM,   4) H3000YG; System, Tomography, Computed, Emission",
    "manufacturer": {
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      "name": "GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING"
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    {
      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-0888-2025/enforcement-record",
      "@type": "schema:Claim",
      "name": "FDA recall Z-0888-2025: GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING is recalling GE Healthcare Infinia I, Model/Catalog Numbers:    1) 5178728,   2) H3000WE,   3) H3000WM,   4) H3000YG; System, Tomography, Computed, Emission",
      "text": "The FDA logged enforcement record Z-0888-2025: GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING is voluntarily recalling GE Healthcare Infinia I, Model/Catalog Numbers:    1) 5178728,   2) H3000WE,   3) H3000WM,   4) H3000YG; System, Tomography, Computed, Emission — reason: GE HealthCare has become aware that certain Infinia, VariCam/VG/VH, Brivo NM 615, Discovery NM 630, Discovery NM/CT 670, and Optima NM/CT 640 Nuclear Medicine systems (see Affected Products Details and Appendices) could have been transported or relocated without proper detector support, which can result in excessive load being applied to the detector mounting mechanisms. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.. Status: Ongoing — the recall is still being carried out.. Initiated 2024-12-18. Affected lots/codes: 1) 5178728:  UDI/DI N/A, System ID YN1200, Serial Number:  16179; System ID YN1650, Serial Number:  17339.      2) H3000WE:   UDI/DI N/A, System ID 82426060010, Serial Number Not Available; System ID 82426080021, Serial Number Not Available; System ID 82426090035, Serial Number 18605; System ID 82426090037, Serial Number 18604; System ID 82426100057, Serial Number 19191; System ID 82426150036, Serial Number 18624; System ID 82426150038, Serial Number Not Available; System ID 82426180015, Serial Number 18611; System ID 082426010021, Serial Number 18644; System ID 082426030032, Serial Number 18627; System ID 082426050012, Serial Number 18629; System ID 082426070041, Serial Number 18639; System ID 082426090044, Serial Number 18652; System ID 082426100067, Serial Number 18648; System ID 082426100069, Serial Number 18641; System ID 082426120031, Serial Number 18656; System ID 082426120033, Serial Number 18650; System ID 082426140029, Serial Number 18628; System ID 082426140030, Serial Number 18647; System ID 082426150039, Serial Number 18651; System ID 082426150040, Serial Number 18657; System ID 082426160040, Serial Number 18442; System ID 082426160054, Serial Number 18645; System ID 082426170004, Serial Number 18649; System ID 082426190031, Serial Number 18646; System ID 082426210028, Serial Number 18655; System ID 082426230028, Serial Number 18653; System ID 082426250006, Serial Number 18637; System ID 671USNHINF, Serial Number 17799; System ID A5128757, Serial Number 17566; System ID 713794INF, Serial Number 17219; System ID 920794inf, Serial Number 16364.    3) H3000WM:  UDI/DI N/A, System ID NM16353, Serial Number 16353; System ID YN1540, Serial Number 16335; System ID YN1555, Serial Number 16315.    4) H3000YG:  UDI/DI N/A, System ID A5172908, Serial Number 16143.. A RECORDED FDA enforcement action (occurred=true).",
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        "sourceUrl": "https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=Z-0888-2025&lang=eng",
        "value": "Devices recall, status Ongoing",
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          "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-0888-2025&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-0888-2025/fda-classification",
      "@type": "schema:Claim",
      "name": "FDA classified recall Z-0888-2025 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.",
      "claimType": "regulatory_determination",
      "reviewStatus": "current",
      "commercialInfluence": false,
      "epistemicStatus": {
        "occurred": false,
        "supported": true,
        "adjudged": true,
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        "source": "U.S. FDA recall classification (openFDA enforcement)",
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        "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-0888-2025&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-0888-2025/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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        "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-0888-2025",
      "numberOfItems": 9,
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          "item": {
            "Field": "Recall number",
            "Value": "Z-0888-2025",
            "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 II",
            "Status": "determination"
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          "position": 4,
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            "Field": "Status",
            "Value": "Ongoing — the recall is still being carried out.",
            "Status": "recorded"
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          "position": 5,
          "item": {
            "Field": "Recalling firm",
            "Value": "GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING",
            "Status": "recorded"
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          "position": 6,
          "item": {
            "Field": "Reason",
            "Value": "GE HealthCare has become aware that certain Infinia, VariCam/VG/VH, Brivo NM 615, Discovery NM 630, Discovery NM/CT 670, and Optima NM/CT 640 Nuclear Medicine systems (see Affected Products Details and Appendices) could have been transported or relocated without proper detector support, which can result in excessive load being applied to the detector mounting mechanisms. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 7,
          "item": {
            "Field": "Initiated",
            "Value": "2024-12-18",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 8,
          "item": {
            "Field": "Lot/code info",
            "Value": "1) 5178728:  UDI/DI N/A, System ID YN1200, Serial Number:  16179; System ID YN1650, Serial Number:  17339.      2) H3000WE:   UDI/DI N/A, System ID 82426060010, Serial Number Not Available; System ID 82426080021, Serial Number Not Available; System ID 82426090035, Serial Number 18605; System ID 82426090037, Serial Number 18604; System ID 82426100057, Serial Number 19191; System ID 82426150036, Serial Number 18624; System ID 82426150038, Serial Number Not Available; System ID 82426180015, Serial Number 18611; System ID 082426010021, Serial Number 18644; System ID 082426030032, Serial Number 18627; System ID 082426050012, Serial Number 18629; System ID 082426070041, Serial Number 18639; System ID 082426090044, Serial Number 18652; System ID 082426100067, Serial Number 18648; System ID 082426100069, Serial Number 18641; System ID 082426120031, Serial Number 18656; System ID 082426120033, Serial Number 18650; System ID 082426140029, Serial Number 18628; System ID 082426140030, Serial Number 18647; System ID 082426150039, Serial Number 18651; System ID 082426150040, Serial Number 18657; System ID 082426160040, Serial Number 18442; System ID 082426160054, Serial Number 18645; System ID 082426170004, Serial Number 18649; System ID 082426190031, Serial Number 18646; System ID 082426210028, Serial Number 18655; System ID 082426230028, Serial Number 18653; System ID 082426250006, Serial Number 18637; System ID 671USNHINF, Serial Number 17799; System ID A5128757, Serial Number 17566; System ID 713794INF, Serial Number 17219; System ID 920794inf, Serial Number 16364.    3) H3000WM:  UDI/DI N/A, System ID NM16353, Serial Number 16353; System ID YN1540, Serial Number 16335; System ID YN1555, Serial Number 16315.    4) H3000YG:  UDI/DI N/A, System ID A5172908, Serial Number 16143.",
            "Status": "recorded"
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          "position": 9,
          "item": {
            "Field": "Distribution pattern",
            "Value": "Worldwide",
            "Status": "recorded"
          }
        }
      ]
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  ]
}