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  "name": "Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel.  Labeled as the following:     a. ANGIO, Model Number: DYNJ905151A;       b. ANGIO/VENO PACK, Model Number: DYNJ58346A;     c. ANGIOGRAPHIC PACK, Model Number: DYNJ57442C, DYNJ64081A;    d. ANGIOGRAPHY PACK, Model Number: DYNJ65963;       e. ANGIOPLASTY PACK-LF, Model Number: DYNJ64655;       f. ARTHROGRAM TRAY, Model Number: SPEC0232;       g. BASIC CATH/ANGIO, Model Number: DYNJ62591A;       h. BASIC PACK, Model Number: DYNJ39752A;       i. C.I.C.N. ANGIO PACK, Model Number: DYNJ53064B;       j. CATH ANGIO PACK, Model Number: DYNJ64050;       k. DBD-KIT NEURO CAROTID SETUP, Model Number: DYKMBNDL148;       l. DBS PACK-LF, Model Number: DYNJ0878178I;       m. GENERAL ANGIO PACK, Model Number: DYNJ57760A;       n. GHIASSI NEURO ANGIO PACK-LF, Model Number: DYNJ57032C;       o. IR NEURO PACK, Model Number: DYNJ39198L, DYNJ39198N;       p. KIT OR AORTOGRM ANGIOPLAST PHT, Model Number: DYNJ906086A;       q. MAIN BASIC NEURO, Model Number: DYNJ908260;       r. NEURO ACCESSORY PACK, Model Number: DYNJ66790, DYNJ66790A, DYNJ66790B;       s. NEURO CATH PACK, Model Number: DYNJ69129, DYNJ83090;       t. NEURO IR PACK, Model Number: DYNJ35066I, DYNJ35066J, DYNJ60701A, DYNJ60701B, DYNJ60701C;       u. NEURO PACK, Model Number: DYNJ43934A, DYNJ61798D, DYNJ66241, DYNJ66241A, DYNJ66241B, DYNJ66241C, DYNJ66241D, DYNJ68956A, DYNJ68956B;        v. NEURO RADIOLOGY PACK, Model Number: DYNJ51107A, DYNJ59903A, DYNJ59903B;       w. NEURO TRAY, Model Number: DYNJ67075, DYNJ67075A;       x. PACK PERCUTANEOUS ANGIO CHRG, Model Number: DYNJ60112A;       y. PEDI ANGIO PACK-LF, Model Number: PHS41743B;       z. PEDIATRIC CATH ANGIO PACK, Model Number: DYNJ54755C;       aa. RADIOLOGY NEURO DRAPE PAC, Model Number: DYNJ61449;       bb. RO-DIEP PACK, Model Number: DYNJ82393A;",
  "description": "FDA recall Z-2331-2023 — MEDLINE INDUSTRIES, LP - Northfield is recalling Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel.  Labeled as the following:     a. ANGIO, Model Number: DYNJ905151A;       b. ANGIO/VENO PACK, Model Number: DYNJ58346A;     c. ANGIOGRAPHIC PACK, Model Number: DYNJ57442C, DYNJ64081A;    d. ANGIOGRAPHY PACK, Model Number: DYNJ65963;       e. ANGIOPLASTY PACK-LF, Model Number: DYNJ64655;       f. ARTHROGRAM TRAY, Model Number: SPEC0232;       g. BASIC CATH/ANGIO, Model Number: DYNJ62591A;       h. BASIC PACK, Model Number: DYNJ39752A;       i. C.I.C.N. ANGIO PACK, Model Number: DYNJ53064B;       j. CATH ANGIO PACK, Model Number: DYNJ64050;       k. DBD-KIT NEURO CAROTID SETUP, Model Number: DYKMBNDL148;       l. DBS PACK-LF, Model Number: DYNJ0878178I;       m. GENERAL ANGIO PACK, Model Number: DYNJ57760A;       n. GHIASSI NEURO ANGIO PACK-LF, Model Number: DYNJ57032C;       o. IR NEURO PACK, Model Number: DYNJ39198L, DYNJ39198N;       p. KIT OR AORTOGRM ANGIOPLAST PHT, Model Number: DYNJ906086A;       q. MAIN BASIC NEURO, Model Number: DYNJ908260;       r. NEURO ACCESSORY PACK, Model Number: DYNJ66790, DYNJ66790A, DYNJ66790B;       s. NEURO CATH PACK, Model Number: DYNJ69129, DYNJ83090;       t. NEURO IR PACK, Model Number: DYNJ35066I, DYNJ35066J, DYNJ60701A, DYNJ60701B, DYNJ60701C;       u. NEURO PACK, Model Number: DYNJ43934A, DYNJ61798D, DYNJ66241, DYNJ66241A, DYNJ66241B, DYNJ66241C, DYNJ66241D, DYNJ68956A, DYNJ68956B;        v. NEURO RADIOLOGY PACK, Model Number: DYNJ51107A, DYNJ59903A, DYNJ59903B;       w. NEURO TRAY, Model Number: DYNJ67075, DYNJ67075A;       x. PACK PERCUTANEOUS ANGIO CHRG, Model Number: DYNJ60112A;       y. PEDI ANGIO PACK-LF, Model Number: PHS41743B;       z. PEDIATRIC CATH ANGIO PACK, Model Number: DYNJ54755C;       aa. RADIOLOGY NEURO DRAPE PAC, Model Number: DYNJ61449;       bb. RO-DIEP PACK, Model Number: DYNJ82393A; (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": "Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel.  Labeled as the following:     a. ANGIO, Model Number: DYNJ905151A;       b. ANGIO/VENO PACK, Model Number: DYNJ58346A;     c. ANGIOGRAPHIC PACK, Model Number: DYNJ57442C, DYNJ64081A;    d. ANGIOGRAPHY PACK, Model Number: DYNJ65963;       e. ANGIOPLASTY PACK-LF, Model Number: DYNJ64655;       f. ARTHROGRAM TRAY, Model Number: SPEC0232;       g. BASIC CATH/ANGIO, Model Number: DYNJ62591A;       h. BASIC PACK, Model Number: DYNJ39752A;       i. C.I.C.N. ANGIO PACK, Model Number: DYNJ53064B;       j. CATH ANGIO PACK, Model Number: DYNJ64050;       k. DBD-KIT NEURO CAROTID SETUP, Model Number: DYKMBNDL148;       l. DBS PACK-LF, Model Number: DYNJ0878178I;       m. GENERAL ANGIO PACK, Model Number: DYNJ57760A;       n. GHIASSI NEURO ANGIO PACK-LF, Model Number: DYNJ57032C;       o. IR NEURO PACK, Model Number: DYNJ39198L, DYNJ39198N;       p. KIT OR AORTOGRM ANGIOPLAST PHT, Model Number: DYNJ906086A;       q. MAIN BASIC NEURO, Model Number: DYNJ908260;       r. NEURO ACCESSORY PACK, Model Number: DYNJ66790, DYNJ66790A, DYNJ66790B;       s. NEURO CATH PACK, Model Number: DYNJ69129, DYNJ83090;       t. NEURO IR PACK, Model Number: DYNJ35066I, DYNJ35066J, DYNJ60701A, DYNJ60701B, DYNJ60701C;       u. NEURO PACK, Model Number: DYNJ43934A, DYNJ61798D, DYNJ66241, DYNJ66241A, DYNJ66241B, DYNJ66241C, DYNJ66241D, DYNJ68956A, DYNJ68956B;        v. NEURO RADIOLOGY PACK, Model Number: DYNJ51107A, DYNJ59903A, DYNJ59903B;       w. NEURO TRAY, Model Number: DYNJ67075, DYNJ67075A;       x. PACK PERCUTANEOUS ANGIO CHRG, Model Number: DYNJ60112A;       y. PEDI ANGIO PACK-LF, Model Number: PHS41743B;       z. PEDIATRIC CATH ANGIO PACK, Model Number: DYNJ54755C;       aa. RADIOLOGY NEURO DRAPE PAC, Model Number: DYNJ61449;       bb. RO-DIEP PACK, Model Number: DYNJ82393A;",
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    {
      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-2331-2023/enforcement-record",
      "@type": "schema:Claim",
      "name": "FDA recall Z-2331-2023: MEDLINE INDUSTRIES, LP - Northfield is recalling Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel.  Labeled as the following:     a. ANGIO, Model Number: DYNJ905151A;       b. ANGIO/VENO PACK, Model Number: DYNJ58346A;     c. ANGIOGRAPHIC PACK, Model Number: DYNJ57442C, DYNJ64081A;    d. ANGIOGRAPHY PACK, Model Number: DYNJ65963;       e. ANGIOPLASTY PACK-LF, Model Number: DYNJ64655;       f. ARTHROGRAM TRAY, Model Number: SPEC0232;       g. BASIC CATH/ANGIO, Model Number: DYNJ62591A;       h. BASIC PACK, Model Number: DYNJ39752A;       i. C.I.C.N. ANGIO PACK, Model Number: DYNJ53064B;       j. CATH ANGIO PACK, Model Number: DYNJ64050;       k. DBD-KIT NEURO CAROTID SETUP, Model Number: DYKMBNDL148;       l. DBS PACK-LF, Model Number: DYNJ0878178I;       m. GENERAL ANGIO PACK, Model Number: DYNJ57760A;       n. GHIASSI NEURO ANGIO PACK-LF, Model Number: DYNJ57032C;       o. IR NEURO PACK, Model Number: DYNJ39198L, DYNJ39198N;       p. KIT OR AORTOGRM ANGIOPLAST PHT, Model Number: DYNJ906086A;       q. MAIN BASIC NEURO, Model Number: DYNJ908260;       r. NEURO ACCESSORY PACK, Model Number: DYNJ66790, DYNJ66790A, DYNJ66790B;       s. NEURO CATH PACK, Model Number: DYNJ69129, DYNJ83090;       t. NEURO IR PACK, Model Number: DYNJ35066I, DYNJ35066J, DYNJ60701A, DYNJ60701B, DYNJ60701C;       u. NEURO PACK, Model Number: DYNJ43934A, DYNJ61798D, DYNJ66241, DYNJ66241A, DYNJ66241B, DYNJ66241C, DYNJ66241D, DYNJ68956A, DYNJ68956B;        v. NEURO RADIOLOGY PACK, Model Number: DYNJ51107A, DYNJ59903A, DYNJ59903B;       w. NEURO TRAY, Model Number: DYNJ67075, DYNJ67075A;       x. PACK PERCUTANEOUS ANGIO CHRG, Model Number: DYNJ60112A;       y. PEDI ANGIO PACK-LF, Model Number: PHS41743B;       z. PEDIATRIC CATH ANGIO PACK, Model Number: DYNJ54755C;       aa. RADIOLOGY NEURO DRAPE PAC, Model Number: DYNJ61449;       bb. RO-DIEP PACK, Model Number: DYNJ82393A;",
      "text": "The FDA logged enforcement record Z-2331-2023: MEDLINE INDUSTRIES, LP - Northfield is voluntarily recalling Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel.  Labeled as the following:     a. ANGIO, Model Number: DYNJ905151A;       b. ANGIO/VENO PACK, Model Number: DYNJ58346A;     c. ANGIOGRAPHIC PACK, Model Number: DYNJ57442C, DYNJ64081A;    d. ANGIOGRAPHY PACK, Model Number: DYNJ65963;       e. ANGIOPLASTY PACK-LF, Model Number: DYNJ64655;       f. ARTHROGRAM TRAY, Model Number: SPEC0232;       g. BASIC CATH/ANGIO, Model Number: DYNJ62591A;       h. BASIC PACK, Model Number: DYNJ39752A;       i. C.I.C.N. ANGIO PACK, Model Number: DYNJ53064B;       j. CATH ANGIO PACK, Model Number: DYNJ64050;       k. DBD-KIT NEURO CAROTID SETUP, Model Number: DYKMBNDL148;       l. DBS PACK-LF, Model Number: DYNJ0878178I;       m. GENERAL ANGIO PACK, Model Number: DYNJ57760A;       n. GHIASSI NEURO ANGIO PACK-LF, Model Number: DYNJ57032C;       o. IR NEURO PACK, Model Number: DYNJ39198L, DYNJ39198N;       p. KIT OR AORTOGRM ANGIOPLAST PHT, Model Number: DYNJ906086A;       q. MAIN BASIC NEURO, Model Number: DYNJ908260;       r. NEURO ACCESSORY PACK, Model Number: DYNJ66790, DYNJ66790A, DYNJ66790B;       s. NEURO CATH PACK, Model Number: DYNJ69129, DYNJ83090;       t. NEURO IR PACK, Model Number: DYNJ35066I, DYNJ35066J, DYNJ60701A, DYNJ60701B, DYNJ60701C;       u. NEURO PACK, Model Number: DYNJ43934A, DYNJ61798D, DYNJ66241, DYNJ66241A, DYNJ66241B, DYNJ66241C, DYNJ66241D, DYNJ68956A, DYNJ68956B;        v. NEURO RADIOLOGY PACK, Model Number: DYNJ51107A, DYNJ59903A, DYNJ59903B;       w. NEURO TRAY, Model Number: DYNJ67075, DYNJ67075A;       x. PACK PERCUTANEOUS ANGIO CHRG, Model Number: DYNJ60112A;       y. PEDI ANGIO PACK-LF, Model Number: PHS41743B;       z. PEDIATRIC CATH ANGIO PACK, Model Number: DYNJ54755C;       aa. RADIOLOGY NEURO DRAPE PAC, Model Number: DYNJ61449;       bb. RO-DIEP PACK, Model Number: DYNJ82393A; — reason: Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.. Status: Ongoing — the recall is still being carried out.. Initiated 2023-05-15. Affected lots/codes: All lot numbers for the following models and corresponding UPCs distributed from Medline between 04/01/2020 and 04/28/2023:    a. Model Number: DYNJ905151A, UPC Number: 019348981341.   b. Model Number: DYNJ58346A, UPC Number: 019348977463.   c. Model Number: DYNJ57442C, UPC Number: 019348920853; Model Number: DYNJ64081A, UPC Number: 019348927374.   d. Model Number: DYNJ65963, UPC Number: 019348930770.   e. Model Number: DYNJ64655, UPC Number: 019348921040.   f. Model Number: SPEC0232, UPC Number: 088827750741.   g. Model Number: DYNJ62591A, UPC Number: 019348979331.   h. Model Number: DYNJ39752A, UPC Number: 088438990723.   i. Model Number: DYNJ53064B, UPC Number: 019348978916.   j. Model Number: DYNJ64050, UPC Number: 019348978046.   k. Model Number: DYKMBNDL148, UPC Number: 019348947839.   l. Model Number: DYNJ0878178I, UPC Number: 019348956435.   m. Model Number: DYNJ57760A, UPC Number: 019348922023.   n. Model Number: DYNJ57032C, UPC Number: 019348945147.    o. Model Number: DYNJ39198L, UPC Number: 019348956435 Model Number: DYNJ39198N, UPC Number: 019532710200.   p. Model Number: DYNJ906086A, UPC Number: 019348920868.   q. Model Number: DYNJ908260, UPC Number: 019532701744.   r. Model Number: DYNJ66790, UPC Number: 019348938243; Model Number: DYNJ66790A, UPC Number: 019348992247; Model Number: DYNJ66790B, UPC Number: 019532709926.   s. Model Number: DYNJ69129, UPC Number: 019348989241; Model Number: DYNJ83090, UPC Number: 019532723093.   t. Model Number: DYNJ35066I, UPC Number: 019348956435; Model Number: DYNJ35066J, UPC Number: 019532709107; Model Number: DYNJ60701A, UPC Number: 019348969378; Model Number: DYNJ60701B, UPC Number: 019348987733; Model Number: DYNJ60701C, UPC Number: 019532703379.   u. Model Number: DYNJ43934A, UPC Number: 019348973360; Model Number: DYNJ61798D, UPC Number: 019348999263; Model Number: DYNJ66241, UPC Number: 019348932296; Model Number: DYNJ66241A, UPC Number: 019348993803; Model Number: DYNJ66241B, UPC Number: 019532705348; Model Number: DYNJ66241C, UPC Number: 019532709685; Model Number: DYNJ66241D, UPC Number: 019532713837; Model Number: DYNJ68956A, UPC Number: 019348987629; Model Number: DYNJ68956B, UPC Number: 019532709434.   v. Model Number: DYNJ51107A, UPC Number: 019348971558; Model Number: DYNJ59903A, UPC Number: 019532704286; Model Number: DYNJ59903B, UPC Number: 019532713120.   w. Model Number: DYNJ67075, UPC Number: 019348938847; Model Number: DYNJ67075A, UPC Number: 019532705453.   x. Model Number: DYNJ60112A, UPC Number: 019348924703.   y. Model Number: PHS41743B, UPC Number: 019348978493.   z. Model Number: DYNJ54755C, UPC Number: 019348977837.   aa. Model Number: DYNJ61449, UPC Number: 019348956734.   bb. Model Number: DYNJ82393A, UPC Number: 019532729232.. A RECORDED FDA enforcement action (occurred=true).",
      "claimType": "official_fact",
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        "sourceUrl": "https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=Z-2331-2023&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-2331-2023&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-2331-2023/fda-classification",
      "@type": "schema:Claim",
      "name": "FDA classified recall Z-2331-2023 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,
        "operative": true
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      "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-2331-2023&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-2331-2023&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-2331-2023/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-2331-2023",
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            "Value": "Z-2331-2023",
            "Status": "recorded"
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            "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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          "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": "MEDLINE INDUSTRIES, LP - Northfield",
            "Status": "recorded"
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            "Field": "Reason",
            "Value": "Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.",
            "Status": "recorded"
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            "Field": "Initiated",
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            "Status": "recorded"
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          "item": {
            "Field": "Lot/code info",
            "Value": "All lot numbers for the following models and corresponding UPCs distributed from Medline between 04/01/2020 and 04/28/2023:    a. Model Number: DYNJ905151A, UPC Number: 019348981341.   b. Model Number: DYNJ58346A, UPC Number: 019348977463.   c. Model Number: DYNJ57442C, UPC Number: 019348920853; Model Number: DYNJ64081A, UPC Number: 019348927374.   d. Model Number: DYNJ65963, UPC Number: 019348930770.   e. Model Number: DYNJ64655, UPC Number: 019348921040.   f. Model Number: SPEC0232, UPC Number: 088827750741.   g. Model Number: DYNJ62591A, UPC Number: 019348979331.   h. Model Number: DYNJ39752A, UPC Number: 088438990723.   i. Model Number: DYNJ53064B, UPC Number: 019348978916.   j. Model Number: DYNJ64050, UPC Number: 019348978046.   k. Model Number: DYKMBNDL148, UPC Number: 019348947839.   l. Model Number: DYNJ0878178I, UPC Number: 019348956435.   m. Model Number: DYNJ57760A, UPC Number: 019348922023.   n. Model Number: DYNJ57032C, UPC Number: 019348945147.    o. Model Number: DYNJ39198L, UPC Number: 019348956435 Model Number: DYNJ39198N, UPC Number: 019532710200.   p. Model Number: DYNJ906086A, UPC Number: 019348920868.   q. Model Number: DYNJ908260, UPC Number: 019532701744.   r. Model Number: DYNJ66790, UPC Number: 019348938243; Model Number: DYNJ66790A, UPC Number: 019348992247; Model Number: DYNJ66790B, UPC Number: 019532709926.   s. Model Number: DYNJ69129, UPC Number: 019348989241; Model Number: DYNJ83090, UPC Number: 019532723093.   t. Model Number: DYNJ35066I, UPC Number: 019348956435; Model Number: DYNJ35066J, UPC Number: 019532709107; Model Number: DYNJ60701A, UPC Number: 019348969378; Model Number: DYNJ60701B, UPC Number: 019348987733; Model Number: DYNJ60701C, UPC Number: 019532703379.   u. Model Number: DYNJ43934A, UPC Number: 019348973360; Model Number: DYNJ61798D, UPC Number: 019348999263; Model Number: DYNJ66241, UPC Number: 019348932296; Model Number: DYNJ66241A, UPC Number: 019348993803; Model Number: DYNJ66241B, UPC Number: 019532705348; Model Number: DYNJ66241C, UPC Number: 019532709685; Model Number: DYNJ66241D, UPC Number: 019532713837; Model Number: DYNJ68956A, UPC Number: 019348987629; Model Number: DYNJ68956B, UPC Number: 019532709434.   v. Model Number: DYNJ51107A, UPC Number: 019348971558; Model Number: DYNJ59903A, UPC Number: 019532704286; Model Number: DYNJ59903B, UPC Number: 019532713120.   w. Model Number: DYNJ67075, UPC Number: 019348938847; Model Number: DYNJ67075A, UPC Number: 019532705453.   x. Model Number: DYNJ60112A, UPC Number: 019348924703.   y. Model Number: PHS41743B, UPC Number: 019348978493.   z. Model Number: DYNJ54755C, UPC Number: 019348977837.   aa. Model Number: DYNJ61449, UPC Number: 019348956734.   bb. Model Number: DYNJ82393A, UPC Number: 019532729232.",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 9,
          "item": {
            "Field": "Distribution pattern",
            "Value": "Worldwide distribution - US Nationwide and the countries of Canada, China, Costa Rica, India, Lebanon, Panama, Qatar, Saudi Arabia, Singapore, United Arab Emirates.",
            "Status": "recorded"
          }
        }
      ]
    }
  ]
}