{
  "@context": {
    "schema": "https://schema.org/",
    "au": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/vocab/agent-native#",
    "@vocab": "https://schema.org/",
    "claims": {
      "@id": "au:claims",
      "@container": "@list"
    },
    "epistemicStatus": "au:epistemicStatus",
    "occurred": "au:occurred",
    "supported": "au:supported",
    "adjudged": "au:adjudged",
    "operative": "au:operative",
    "grounding": "au:grounding",
    "groundingType": "au:groundingType",
    "adjudicator": "au:adjudicator",
    "source": "au:source",
    "sourceUrl": "au:sourceUrl",
    "value": "au:value",
    "claimType": "au:claimType",
    "reviewStatus": "au:reviewStatus",
    "commercialInfluence": "au:commercialInfluence",
    "falsifier": "au:falsifier"
  },
  "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-1578-2025.jsonld",
  "@type": "schema:Dataset",
  "name": "Brand Name: Rover  Product Name: Mobile X-ray System  Model/Catalog Number: MXU-RV71  Product Description: Rover Mobile X-rays System (\"Rover\") is a mobile imaging system that incorporates a self-contained X-ray generator,  imaging display and software for acquiring medical diagnostic images outside a standard X-ray room. It is designed specifically for Digital Radiography (DR) with vendor-supported detectors.  The Rover is designed to perform radiographic X-ray examinations for disease/injury detection, diagnosis, medical and surgical treatment planning, and therapy monitoring, where patient condition contraindicates transport to a fixed X-ray unit The Rover can be used on pediatric and adult patients, in all patient treatment areas  Component: N/A",
  "description": "FDA recall Z-1578-2025 — Micro-X Ltd. is recalling Brand Name: Rover  Product Name: Mobile X-ray System  Model/Catalog Number: MXU-RV71  Product Description: Rover Mobile X-rays System (\"Rover\") is a mobile imaging system that incorporates a self-contained X-ray generator,  imaging display and software for acquiring medical diagnostic images outside a standard X-ray room. It is designed specifically for Digital Radiography (DR) with vendor-supported detectors.  The Rover is designed to perform radiographic X-ray examinations for disease/injury detection, diagnosis, medical and surgical treatment planning, and therapy monitoring, where patient condition contraindicates transport to a fixed X-ray unit The Rover can be used on pediatric and adult patients, in all patient treatment areas  Component: N/A (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/",
  "isAccessibleForFree": true,
  "isPartOf": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/",
  "rdfs:isDefinedBy": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/vocab/agent-native",
  "seeAlso": "https://agenticu.ryanjhunter.workers.dev/commons/the-research-object",
  "dateModified": "2026-06-24T07:02:03.626072+00:00",
  "isBasedOn": {
    "@type": "schema:Dataset",
    "name": "openFDA drug & device enforcement (recall) reports",
    "url": "https://open.fda.gov/apis/drug/enforcement/",
    "creator": {
      "@type": "schema:GovernmentOrganization",
      "name": "U.S. Food & Drug Administration"
    }
  },
  "sameAs": "https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=Z-1578-2025&lang=eng",
  "about": {
    "@type": "schema:MedicalDevice",
    "name": "Brand Name: Rover  Product Name: Mobile X-ray System  Model/Catalog Number: MXU-RV71  Product Description: Rover Mobile X-rays System (\"Rover\") is a mobile imaging system that incorporates a self-contained X-ray generator,  imaging display and software for acquiring medical diagnostic images outside a standard X-ray room. It is designed specifically for Digital Radiography (DR) with vendor-supported detectors.  The Rover is designed to perform radiographic X-ray examinations for disease/injury detection, diagnosis, medical and surgical treatment planning, and therapy monitoring, where patient condition contraindicates transport to a fixed X-ray unit The Rover can be used on pediatric and adult patients, in all patient treatment areas  Component: N/A",
    "manufacturer": {
      "@type": "schema:Organization",
      "name": "Micro-X Ltd."
    }
  },
  "claims": [
    {
      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-1578-2025/enforcement-record",
      "@type": "schema:Claim",
      "name": "FDA recall Z-1578-2025: Micro-X Ltd. is recalling Brand Name: Rover  Product Name: Mobile X-ray System  Model/Catalog Number: MXU-RV71  Product Description: Rover Mobile X-rays System (\"Rover\") is a mobile imaging system that incorporates a self-contained X-ray generator,  imaging display and software for acquiring medical diagnostic images outside a standard X-ray room. It is designed specifically for Digital Radiography (DR) with vendor-supported detectors.  The Rover is designed to perform radiographic X-ray examinations for disease/injury detection, diagnosis, medical and surgical treatment planning, and therapy monitoring, where patient condition contraindicates transport to a fixed X-ray unit The Rover can be used on pediatric and adult patients, in all patient treatment areas  Component: N/A",
      "text": "The FDA logged enforcement record Z-1578-2025: Micro-X Ltd. is voluntarily recalling Brand Name: Rover  Product Name: Mobile X-ray System  Model/Catalog Number: MXU-RV71  Product Description: Rover Mobile X-rays System (\"Rover\") is a mobile imaging system that incorporates a self-contained X-ray generator,  imaging display and software for acquiring medical diagnostic images outside a standard X-ray room. It is designed specifically for Digital Radiography (DR) with vendor-supported detectors.  The Rover is designed to perform radiographic X-ray examinations for disease/injury detection, diagnosis, medical and surgical treatment planning, and therapy monitoring, where patient condition contraindicates transport to a fixed X-ray unit The Rover can be used on pediatric and adult patients, in all patient treatment areas  Component: N/A — reason: Potential for early life x-ray tube failure for mobile x-ray system due to excessive thermal load on the anode.. Status: Ongoing — the recall is still being carried out.. Initiated 2025-03-28. Affected lots/codes: Serial Number/UDI: MSN0334 (01)09357123000051(11)220921(21)00334; MSN0350 (01)09357123000037(11)230328(21)00350 ; MSN0352 (01)09357123000051(11)230823(21)00352; MSN0364 01)09357123000051(11)230705(21)00364; MSN0382 (01)09357123000051(11)230809(21)00382; MSN0383 (01)09357123000051(11)230814(21)00383; MSN0384 (01)09357123000051(11)230816(21)00384; MSN0385 (01)09357123000051(11)230906(21)00385; MSN0386 (01)09357123000051(11)230908(21)00386; MSN0387 (01)09357123000051(11)230914(21)00387; MSN0388 (01)09357123000051(11)230916(21)00388; MSN0389 (01)09357123000051(11)230918(21)00389; MSN0390 (01)09357123000051(11)231013(21)00390; MSN0395 (01)09357123000051(11)231106(21)00395; MSN0397 (01)09357123000051(11)231118(21)00397; MSN0399 (01)09357123000051(11)240122(21)00399; MSN0400 (01)09357123000051(11)240207(21)00400; MSN0401 (01)09357123000051(11)240131(21)00401; MSN0402 01)09357123000051(11)240202(21)00402; MSN0403 (01)09357123000051(11)240205(21)00403; MSN0405 (01)09357123000051(11)240206(21)00405; MSN0408 (01)09357123000051(11)240308(21)00408; MSN0409 (01)09357123000051(11)240312(21)00409; MSN0410 (01)09357123000051(11)240318(21)00410; MSN0411 (01)09357123000051(11)240319(21)00411; MSN0422 (01)09357123000051(11)240724(21)00422; MSN0423 (01)09357123000051(11)240808(21)00423; MSN0424 (01)09357123000051(11)240809(21)00424; MSN0425 (01)09357123000051(11)240812(21)00425; MSN0426 (01)09357123000051(11)240812(21)00426; MSN0427 (01)09357123000051(11)240812(21)00427;. 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-1578-2025&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-1578-2025&lang=eng"
        }
      },
      "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-1578-2025/fda-classification",
      "@type": "schema:Claim",
      "name": "FDA classified recall Z-1578-2025 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,
        "operative": true
      },
      "grounding": {
        "groundingType": "AdjudicativeAct",
        "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-1578-2025&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-1578-2025&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-1578-2025/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,
        "operative": true
      },
      "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."
    }
  ],
  "hasPart": [
    {
      "@type": "schema:ItemList",
      "name": "FDA recall details — Z-1578-2025",
      "numberOfItems": 9,
      "itemListElement": [
        {
          "@type": "schema:ListItem",
          "position": 1,
          "item": {
            "Field": "Recall number",
            "Value": "Z-1578-2025",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 2,
          "item": {
            "Field": "Product type",
            "Value": "Devices",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 3,
          "item": {
            "Field": "Classification",
            "Value": "Class II",
            "Status": "determination"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 4,
          "item": {
            "Field": "Status",
            "Value": "Ongoing — the recall is still being carried out.",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 5,
          "item": {
            "Field": "Recalling firm",
            "Value": "Micro-X Ltd.",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 6,
          "item": {
            "Field": "Reason",
            "Value": "Potential for early life x-ray tube failure for mobile x-ray system due to excessive thermal load on the anode.",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 7,
          "item": {
            "Field": "Initiated",
            "Value": "2025-03-28",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 8,
          "item": {
            "Field": "Lot/code info",
            "Value": "Serial Number/UDI: MSN0334 (01)09357123000051(11)220921(21)00334; MSN0350 (01)09357123000037(11)230328(21)00350 ; MSN0352 (01)09357123000051(11)230823(21)00352; MSN0364 01)09357123000051(11)230705(21)00364; MSN0382 (01)09357123000051(11)230809(21)00382; MSN0383 (01)09357123000051(11)230814(21)00383; MSN0384 (01)09357123000051(11)230816(21)00384; MSN0385 (01)09357123000051(11)230906(21)00385; MSN0386 (01)09357123000051(11)230908(21)00386; MSN0387 (01)09357123000051(11)230914(21)00387; MSN0388 (01)09357123000051(11)230916(21)00388; MSN0389 (01)09357123000051(11)230918(21)00389; MSN0390 (01)09357123000051(11)231013(21)00390; MSN0395 (01)09357123000051(11)231106(21)00395; MSN0397 (01)09357123000051(11)231118(21)00397; MSN0399 (01)09357123000051(11)240122(21)00399; MSN0400 (01)09357123000051(11)240207(21)00400; MSN0401 (01)09357123000051(11)240131(21)00401; MSN0402 01)09357123000051(11)240202(21)00402; MSN0403 (01)09357123000051(11)240205(21)00403; MSN0405 (01)09357123000051(11)240206(21)00405; MSN0408 (01)09357123000051(11)240308(21)00408; MSN0409 (01)09357123000051(11)240312(21)00409; MSN0410 (01)09357123000051(11)240318(21)00410; MSN0411 (01)09357123000051(11)240319(21)00411; MSN0422 (01)09357123000051(11)240724(21)00422; MSN0423 (01)09357123000051(11)240808(21)00423; MSN0424 (01)09357123000051(11)240809(21)00424; MSN0425 (01)09357123000051(11)240812(21)00425; MSN0426 (01)09357123000051(11)240812(21)00426; MSN0427 (01)09357123000051(11)240812(21)00427;",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 9,
          "item": {
            "Field": "Distribution pattern",
            "Value": "US Nationwide distribution in the states of CA, NJ, and Puerto Rico (US territory).",
            "Status": "recorded"
          }
        }
      ]
    }
  ]
}