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  "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-2156-2023.jsonld",
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  "name": "Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following:  a)\tBLOCK PACK, Model Number DYNJ81722;   b)\tPAIN BLOCK TRAY, Model Number DYNJRA0827A;   c)\tPAIN PREP TRAY W/PROBE COVER, Model Number DYNJRA0881;   d)\tPAIN PREP TRAY W/PROBE COVER, Model Number DYNJRA0881A;   e)\tPAIN TRAY, Model Number DYNJRA1603;   f)\tFEMORAL BLOCK TRAY, Model Number DYNJRA1739A;   g)\tTAP BLOCK, Model Number DYNJRA1823;   h)\tNERVE BLOCK PREP TRAY, Model Number DYNJRA1837;   i)\tPAIN PREP TRAY W/PROBE COVER, Model Number DYNJRA1847;   j)\tANESTHESIA BLOCK PACK - TBR, Model Number DYNJRA1864;   k)\t18G CPNB 20G STYLETED CATHETER, Model Number DYNJRA1869;   l)\tNERVE BLOCK TRAY, Model Number DYNJRA1878;   m)\tBLOCK KIT, Model Number DYNJRA1893;   n)\tNERVE BLOCK TRAY, Model Number DYNJRA1900;   o)\tUS TPI KIT, Model Number DYNJRA1945;   p)\tPAIN PREP TRAY W/PROBE COVER, Model Number DYNJRA1975;   q)\tDR LEWIS US TRAY, Model Number DYNJRA1998;   r)\tULTRASOUND GUIDED NERVE BLOCK, Model Number DYNJRA2013;   s)\tULTRASOUND TRAY, Model Number DYNJRA2022;   t)\tNERVE BLOCK INSERTION, Model Number DYNJRA2027;   u)\tPAIN PREP W/ PROBE COVER TRAY, Model Number DYNJRA2028;   v)\tPAIN PREP W/ PROBE COVER TRAY, Model Number DYNJRA2028A;   w)\tPAIN TRAY, Model Number DYNJRA2041;   x)\tSUPPORT TRAY, Model Number DYNJRA2044;   y)\tSUPERFICIAL NERVE BLOCK, Model Number DYNJRA2086;   z)\tNERVE BLOCK TRAY, Model Number DYNJRA2148;   aa)\tTRAY 18G CPNB 20G STYLETED, Model Number DYNJRA9040;   bb)\tULTRASOUND BLOCK TRAY, Model Number DYNJRA9044;   cc)\tPERIPHERAL NERVE CATHETER KT, Model Number PAIN1560;   dd)\tPAIN PREP W/PROBE COVER TRAY, Model Number PAIN1762",
  "description": "FDA recall Z-2156-2023 — MEDLINE INDUSTRIES, LP - Northfield is recalling Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following:  a)\tBLOCK PACK, Model Number DYNJ81722;   b)\tPAIN BLOCK TRAY, Model Number DYNJRA0827A;   c)\tPAIN PREP TRAY W/PROBE COVER, Model Number DYNJRA0881;   d)\tPAIN PREP TRAY W/PROBE COVER, Model Number DYNJRA0881A;   e)\tPAIN TRAY, Model Number DYNJRA1603;   f)\tFEMORAL BLOCK TRAY, Model Number DYNJRA1739A;   g)\tTAP BLOCK, Model Number DYNJRA1823;   h)\tNERVE BLOCK PREP TRAY, Model Number DYNJRA1837;   i)\tPAIN PREP TRAY W/PROBE COVER, Model Number DYNJRA1847;   j)\tANESTHESIA BLOCK PACK - TBR, Model Number DYNJRA1864;   k)\t18G CPNB 20G STYLETED CATHETER, Model Number DYNJRA1869;   l)\tNERVE BLOCK TRAY, Model Number DYNJRA1878;   m)\tBLOCK KIT, Model Number DYNJRA1893;   n)\tNERVE BLOCK TRAY, Model Number DYNJRA1900;   o)\tUS TPI KIT, Model Number DYNJRA1945;   p)\tPAIN PREP TRAY W/PROBE COVER, Model Number DYNJRA1975;   q)\tDR LEWIS US TRAY, Model Number DYNJRA1998;   r)\tULTRASOUND GUIDED NERVE BLOCK, Model Number DYNJRA2013;   s)\tULTRASOUND TRAY, Model Number DYNJRA2022;   t)\tNERVE BLOCK INSERTION, Model Number DYNJRA2027;   u)\tPAIN PREP W/ PROBE COVER TRAY, Model Number DYNJRA2028;   v)\tPAIN PREP W/ PROBE COVER TRAY, Model Number DYNJRA2028A;   w)\tPAIN TRAY, Model Number DYNJRA2041;   x)\tSUPPORT TRAY, Model Number DYNJRA2044;   y)\tSUPERFICIAL NERVE BLOCK, Model Number DYNJRA2086;   z)\tNERVE BLOCK TRAY, Model Number DYNJRA2148;   aa)\tTRAY 18G CPNB 20G STYLETED, Model Number DYNJRA9040;   bb)\tULTRASOUND BLOCK TRAY, Model Number DYNJRA9044;   cc)\tPERIPHERAL NERVE CATHETER KT, Model Number PAIN1560;   dd)\tPAIN PREP W/PROBE COVER TRAY, Model Number PAIN1762 (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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    "@type": "schema:MedicalDevice",
    "name": "Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following:  a)\tBLOCK PACK, Model Number DYNJ81722;   b)\tPAIN BLOCK TRAY, Model Number DYNJRA0827A;   c)\tPAIN PREP TRAY W/PROBE COVER, Model Number DYNJRA0881;   d)\tPAIN PREP TRAY W/PROBE COVER, Model Number DYNJRA0881A;   e)\tPAIN TRAY, Model Number DYNJRA1603;   f)\tFEMORAL BLOCK TRAY, Model Number DYNJRA1739A;   g)\tTAP BLOCK, Model Number DYNJRA1823;   h)\tNERVE BLOCK PREP TRAY, Model Number DYNJRA1837;   i)\tPAIN PREP TRAY W/PROBE COVER, Model Number DYNJRA1847;   j)\tANESTHESIA BLOCK PACK - TBR, Model Number DYNJRA1864;   k)\t18G CPNB 20G STYLETED CATHETER, Model Number DYNJRA1869;   l)\tNERVE BLOCK TRAY, Model Number DYNJRA1878;   m)\tBLOCK KIT, Model Number DYNJRA1893;   n)\tNERVE BLOCK TRAY, Model Number DYNJRA1900;   o)\tUS TPI KIT, Model Number DYNJRA1945;   p)\tPAIN PREP TRAY W/PROBE COVER, Model Number DYNJRA1975;   q)\tDR LEWIS US TRAY, Model Number DYNJRA1998;   r)\tULTRASOUND GUIDED NERVE BLOCK, Model Number DYNJRA2013;   s)\tULTRASOUND TRAY, Model Number DYNJRA2022;   t)\tNERVE BLOCK INSERTION, Model Number DYNJRA2027;   u)\tPAIN PREP W/ PROBE COVER TRAY, Model Number DYNJRA2028;   v)\tPAIN PREP W/ PROBE COVER TRAY, Model Number DYNJRA2028A;   w)\tPAIN TRAY, Model Number DYNJRA2041;   x)\tSUPPORT TRAY, Model Number DYNJRA2044;   y)\tSUPERFICIAL NERVE BLOCK, Model Number DYNJRA2086;   z)\tNERVE BLOCK TRAY, Model Number DYNJRA2148;   aa)\tTRAY 18G CPNB 20G STYLETED, Model Number DYNJRA9040;   bb)\tULTRASOUND BLOCK TRAY, Model Number DYNJRA9044;   cc)\tPERIPHERAL NERVE CATHETER KT, Model Number PAIN1560;   dd)\tPAIN PREP W/PROBE COVER TRAY, Model Number PAIN1762",
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      "name": "MEDLINE INDUSTRIES, LP - Northfield"
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      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-2156-2023/enforcement-record",
      "@type": "schema:Claim",
      "name": "FDA recall Z-2156-2023: MEDLINE INDUSTRIES, LP - Northfield is recalling Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following:  a)\tBLOCK PACK, Model Number DYNJ81722;   b)\tPAIN BLOCK TRAY, Model Number DYNJRA0827A;   c)\tPAIN PREP TRAY W/PROBE COVER, Model Number DYNJRA0881;   d)\tPAIN PREP TRAY W/PROBE COVER, Model Number DYNJRA0881A;   e)\tPAIN TRAY, Model Number DYNJRA1603;   f)\tFEMORAL BLOCK TRAY, Model Number DYNJRA1739A;   g)\tTAP BLOCK, Model Number DYNJRA1823;   h)\tNERVE BLOCK PREP TRAY, Model Number DYNJRA1837;   i)\tPAIN PREP TRAY W/PROBE COVER, Model Number DYNJRA1847;   j)\tANESTHESIA BLOCK PACK - TBR, Model Number DYNJRA1864;   k)\t18G CPNB 20G STYLETED CATHETER, Model Number DYNJRA1869;   l)\tNERVE BLOCK TRAY, Model Number DYNJRA1878;   m)\tBLOCK KIT, Model Number DYNJRA1893;   n)\tNERVE BLOCK TRAY, Model Number DYNJRA1900;   o)\tUS TPI KIT, Model Number DYNJRA1945;   p)\tPAIN PREP TRAY W/PROBE COVER, Model Number DYNJRA1975;   q)\tDR LEWIS US TRAY, Model Number DYNJRA1998;   r)\tULTRASOUND GUIDED NERVE BLOCK, Model Number DYNJRA2013;   s)\tULTRASOUND TRAY, Model Number DYNJRA2022;   t)\tNERVE BLOCK INSERTION, Model Number DYNJRA2027;   u)\tPAIN PREP W/ PROBE COVER TRAY, Model Number DYNJRA2028;   v)\tPAIN PREP W/ PROBE COVER TRAY, Model Number DYNJRA2028A;   w)\tPAIN TRAY, Model Number DYNJRA2041;   x)\tSUPPORT TRAY, Model Number DYNJRA2044;   y)\tSUPERFICIAL NERVE BLOCK, Model Number DYNJRA2086;   z)\tNERVE BLOCK TRAY, Model Number DYNJRA2148;   aa)\tTRAY 18G CPNB 20G STYLETED, Model Number DYNJRA9040;   bb)\tULTRASOUND BLOCK TRAY, Model Number DYNJRA9044;   cc)\tPERIPHERAL NERVE CATHETER KT, Model Number PAIN1560;   dd)\tPAIN PREP W/PROBE COVER TRAY, Model Number PAIN1762",
      "text": "The FDA logged enforcement record Z-2156-2023: MEDLINE INDUSTRIES, LP - Northfield is voluntarily recalling Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following:  a)\tBLOCK PACK, Model Number DYNJ81722;   b)\tPAIN BLOCK TRAY, Model Number DYNJRA0827A;   c)\tPAIN PREP TRAY W/PROBE COVER, Model Number DYNJRA0881;   d)\tPAIN PREP TRAY W/PROBE COVER, Model Number DYNJRA0881A;   e)\tPAIN TRAY, Model Number DYNJRA1603;   f)\tFEMORAL BLOCK TRAY, Model Number DYNJRA1739A;   g)\tTAP BLOCK, Model Number DYNJRA1823;   h)\tNERVE BLOCK PREP TRAY, Model Number DYNJRA1837;   i)\tPAIN PREP TRAY W/PROBE COVER, Model Number DYNJRA1847;   j)\tANESTHESIA BLOCK PACK - TBR, Model Number DYNJRA1864;   k)\t18G CPNB 20G STYLETED CATHETER, Model Number DYNJRA1869;   l)\tNERVE BLOCK TRAY, Model Number DYNJRA1878;   m)\tBLOCK KIT, Model Number DYNJRA1893;   n)\tNERVE BLOCK TRAY, Model Number DYNJRA1900;   o)\tUS TPI KIT, Model Number DYNJRA1945;   p)\tPAIN PREP TRAY W/PROBE COVER, Model Number DYNJRA1975;   q)\tDR LEWIS US TRAY, Model Number DYNJRA1998;   r)\tULTRASOUND GUIDED NERVE BLOCK, Model Number DYNJRA2013;   s)\tULTRASOUND TRAY, Model Number DYNJRA2022;   t)\tNERVE BLOCK INSERTION, Model Number DYNJRA2027;   u)\tPAIN PREP W/ PROBE COVER TRAY, Model Number DYNJRA2028;   v)\tPAIN PREP W/ PROBE COVER TRAY, Model Number DYNJRA2028A;   w)\tPAIN TRAY, Model Number DYNJRA2041;   x)\tSUPPORT TRAY, Model Number DYNJRA2044;   y)\tSUPERFICIAL NERVE BLOCK, Model Number DYNJRA2086;   z)\tNERVE BLOCK TRAY, Model Number DYNJRA2148;   aa)\tTRAY 18G CPNB 20G STYLETED, Model Number DYNJRA9040;   bb)\tULTRASOUND BLOCK TRAY, Model Number DYNJRA9044;   cc)\tPERIPHERAL NERVE CATHETER KT, Model Number PAIN1560;   dd)\tPAIN PREP W/PROBE COVER TRAY, Model Number PAIN1762 — reason: Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.. Status: Ongoing — the recall is still being carried out.. Initiated 2023-05-18. Affected lots/codes: all lots within expiry, distributed from Medline between December 2017 1 May 2023:   a) Model Number DYNJ81722, UDI/DI (EA) 10195327136437, UDI/DI (CS)40195327136438; b) Model Number DYNJRA0827A, UDI/DI (EA) 10193489214468, UDI/DI (CS)40193489214469; c) Model Number DYNJRA0881, UDI/DI (EA) 10889942463930, UDI/DI (CS)40889942463931; d) Model Number DYNJRA0881A, UDI/DI (EA) 10195327262402, UDI/DI (CS)40195327262403; e) Model Number DYNJRA1603, UDI/DI (EA) 10193489299007, UDI/DI (CS)40193489299008; f) Model Number DYNJRA1739A, UDI/DI (EA) 10193489924954, UDI/DI (CS)40193489924955; g) Model Number DYNJRA1823, UDI/DI (EA) 10193489961881, UDI/DI (CS)40193489961882; h) Model Number DYNJRA1837, UDI/DI (EA) 10193489976717, UDI/DI (CS)40193489976718; i) Model Number DYNJRA1847, UDI/DI (EA) 10193489993660, UDI/DI (CS)40193489993661; j) Model Number DYNJRA1864, UDI/DI (EA) 10195327008789, UDI/DI (CS)40195327008780; k) Model Number DYNJRA1869, UDI/DI (EA) 10195327018818, UDI/DI (CS)40195327018819; l) Model Number DYNJRA1878, UDI/DI (EA) 10195327040376, UDI/DI (CS)40195327040377; m) Model Number DYNJRA1893, UDI/DI (EA) 10195327062828, UDI/DI (CS)40195327062829; n) Model Number DYNJRA1900, UDI/DI (EA) 10195327082253, UDI/DI (CS)40195327082254; o) Model Number DYNJRA1945, UDI/DI (EA) 10195327133054, UDI/DI (CS)40195327133055; p) Model Number DYNJRA1975, UDI/DI (EA) 10195327163242, UDI/DI (CS)40195327163243; q) Model Number DYNJRA1998, UDI/DI (EA) 10195327194291, UDI/DI (CS)40195327194292; r) Model Number DYNJRA2013, UDI/DI (EA) 10195327212049, UDI/DI (CS)40195327212040; s) Model Number DYNJRA2022, UDI/DI (EA) 10195327218164, UDI/DI (CS)40195327218165; t) Model Number DYNJRA2027, UDI/DI (EA) 10195327225223, UDI/DI (CS)40195327225224; u) Model Number DYNJRA2028, UDI/DI (EA) 10195327226299, UDI/DI (CS)40195327226290; v) Model Number DYNJRA2028A, UDI/DI (EA) 10195327352042, UDI/DI (CS)40195327352043; w) Model Number DYNJRA2041, UDI/DI (EA) 10195327243708, UDI/DI (CS)40195327243709; x) Model Number DYNJRA2044, UDI/DI (EA) 10195327247300, UDI/DI (CS)40195327247301; y) Model Number DYNJRA2086, UDI/DI (EA) 10195327286750, UDI/DI (CS)40195327286751; z) Model Number DYNJRA2148, UDI/DI (EA) 10195327363758, UDI/DI (CS)40195327363759; aa) Model Number DYNJRA9040, UDI/DI (EA) 10193489830514, UDI/DI (CS)40193489830515; bb) Model Number DYNJRA9044, UDI/DI (EA) 10193489888119, UDI/DI (CS)40193489888110; cc) Model Number PAIN1560, UDI/DI (EA) 10193489215380, UDI/DI (CS)40193489215381; dd) Model Number PAIN1762, UDI/DI (EA) 10193489962093, UDI/DI (CS)40193489962094;. A RECORDED FDA enforcement action (occurred=true).",
      "claimType": "official_fact",
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        "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-2156-2023&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-2156-2023&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-2156-2023/fda-classification",
      "@type": "schema:Claim",
      "name": "FDA classified recall Z-2156-2023 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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      "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-2156-2023&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-2156-2023&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-2156-2023/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."
    }
  ],
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      "name": "FDA recall details — Z-2156-2023",
      "numberOfItems": 9,
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          "position": 1,
          "item": {
            "Field": "Recall number",
            "Value": "Z-2156-2023",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "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,
          "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": "MEDLINE INDUSTRIES, LP - Northfield",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 6,
          "item": {
            "Field": "Reason",
            "Value": "Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.",
            "Status": "recorded"
          }
        },
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          "@type": "schema:ListItem",
          "position": 7,
          "item": {
            "Field": "Initiated",
            "Value": "2023-05-18",
            "Status": "recorded"
          }
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          "position": 8,
          "item": {
            "Field": "Lot/code info",
            "Value": "all lots within expiry, distributed from Medline between December 2017 1 May 2023:   a) Model Number DYNJ81722, UDI/DI (EA) 10195327136437, UDI/DI (CS)40195327136438; b) Model Number DYNJRA0827A, UDI/DI (EA) 10193489214468, UDI/DI (CS)40193489214469; c) Model Number DYNJRA0881, UDI/DI (EA) 10889942463930, UDI/DI (CS)40889942463931; d) Model Number DYNJRA0881A, UDI/DI (EA) 10195327262402, UDI/DI (CS)40195327262403; e) Model Number DYNJRA1603, UDI/DI (EA) 10193489299007, UDI/DI (CS)40193489299008; f) Model Number DYNJRA1739A, UDI/DI (EA) 10193489924954, UDI/DI (CS)40193489924955; g) Model Number DYNJRA1823, UDI/DI (EA) 10193489961881, UDI/DI (CS)40193489961882; h) Model Number DYNJRA1837, UDI/DI (EA) 10193489976717, UDI/DI (CS)40193489976718; i) Model Number DYNJRA1847, UDI/DI (EA) 10193489993660, UDI/DI (CS)40193489993661; j) Model Number DYNJRA1864, UDI/DI (EA) 10195327008789, UDI/DI (CS)40195327008780; k) Model Number DYNJRA1869, UDI/DI (EA) 10195327018818, UDI/DI (CS)40195327018819; l) Model Number DYNJRA1878, UDI/DI (EA) 10195327040376, UDI/DI (CS)40195327040377; m) Model Number DYNJRA1893, UDI/DI (EA) 10195327062828, UDI/DI (CS)40195327062829; n) Model Number DYNJRA1900, UDI/DI (EA) 10195327082253, UDI/DI (CS)40195327082254; o) Model Number DYNJRA1945, UDI/DI (EA) 10195327133054, UDI/DI (CS)40195327133055; p) Model Number DYNJRA1975, UDI/DI (EA) 10195327163242, UDI/DI (CS)40195327163243; q) Model Number DYNJRA1998, UDI/DI (EA) 10195327194291, UDI/DI (CS)40195327194292; r) Model Number DYNJRA2013, UDI/DI (EA) 10195327212049, UDI/DI (CS)40195327212040; s) Model Number DYNJRA2022, UDI/DI (EA) 10195327218164, UDI/DI (CS)40195327218165; t) Model Number DYNJRA2027, UDI/DI (EA) 10195327225223, UDI/DI (CS)40195327225224; u) Model Number DYNJRA2028, UDI/DI (EA) 10195327226299, UDI/DI (CS)40195327226290; v) Model Number DYNJRA2028A, UDI/DI (EA) 10195327352042, UDI/DI (CS)40195327352043; w) Model Number DYNJRA2041, UDI/DI (EA) 10195327243708, UDI/DI (CS)40195327243709; x) Model Number DYNJRA2044, UDI/DI (EA) 10195327247300, UDI/DI (CS)40195327247301; y) Model Number DYNJRA2086, UDI/DI (EA) 10195327286750, UDI/DI (CS)40195327286751; z) Model Number DYNJRA2148, UDI/DI (EA) 10195327363758, UDI/DI (CS)40195327363759; aa) Model Number DYNJRA9040, UDI/DI (EA) 10193489830514, UDI/DI (CS)40193489830515; bb) Model Number DYNJRA9044, UDI/DI (EA) 10193489888119, UDI/DI (CS)40193489888110; cc) Model Number PAIN1560, UDI/DI (EA) 10193489215380, UDI/DI (CS)40193489215381; dd) Model Number PAIN1762, UDI/DI (EA) 10193489962093, UDI/DI (CS)40193489962094;",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 9,
          "item": {
            "Field": "Distribution pattern",
            "Value": "Worldwide Distribution: US (Nationwide) and OUS (foreign) United Arab Emirates, Singapore, Lebanon, China Qatar, Costa Rica, India, Canada, Panama & Saudi Arabia.",
            "Status": "recorded"
          }
        }
      ]
    }
  ]
}