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  "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-2036-2026.jsonld",
  "@type": "schema:Dataset",
  "name": "Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows:   1. ANTERIOR CERVICAL FUSION PACK, Medline Kit Number/SKU DYNJ40566C;   2. OB PACK (OBSJD)642-LF, Medline Kit Number/SKU DYNJ47491F;   3. ANTERIOR CERVICAL-LF, Medline Kit Number/SKU DYNJ58274;   4. ANTERIOR CERVICAL-LF, Medline Kit Number/SKU DYNJ58344;   5. ANTERIOR CERVICAL-LF, Medline Kit Number/SKU DYNJS3016.",
  "description": "FDA recall Z-2036-2026 — Medline Industries, LP is recalling Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows:   1. ANTERIOR CERVICAL FUSION PACK, Medline Kit Number/SKU DYNJ40566C;   2. OB PACK (OBSJD)642-LF, Medline Kit Number/SKU DYNJ47491F;   3. ANTERIOR CERVICAL-LF, Medline Kit Number/SKU DYNJ58274;   4. ANTERIOR CERVICAL-LF, Medline Kit Number/SKU DYNJ58344;   5. ANTERIOR CERVICAL-LF, Medline Kit Number/SKU DYNJS3016. (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/",
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  "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"
    }
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  "sameAs": "https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=Z-2036-2026&lang=eng",
  "about": {
    "@type": "schema:MedicalDevice",
    "name": "Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows:   1. ANTERIOR CERVICAL FUSION PACK, Medline Kit Number/SKU DYNJ40566C;   2. OB PACK (OBSJD)642-LF, Medline Kit Number/SKU DYNJ47491F;   3. ANTERIOR CERVICAL-LF, Medline Kit Number/SKU DYNJ58274;   4. ANTERIOR CERVICAL-LF, Medline Kit Number/SKU DYNJ58344;   5. ANTERIOR CERVICAL-LF, Medline Kit Number/SKU DYNJS3016.",
    "manufacturer": {
      "@type": "schema:Organization",
      "name": "Medline Industries, LP"
    }
  },
  "claims": [
    {
      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-2036-2026/enforcement-record",
      "@type": "schema:Claim",
      "name": "FDA recall Z-2036-2026: Medline Industries, LP is recalling Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows:   1. ANTERIOR CERVICAL FUSION PACK, Medline Kit Number/SKU DYNJ40566C;   2. OB PACK (OBSJD)642-LF, Medline Kit Number/SKU DYNJ47491F;   3. ANTERIOR CERVICAL-LF, Medline Kit Number/SKU DYNJ58274;   4. ANTERIOR CERVICAL-LF, Medline Kit Number/SKU DYNJ58344;   5. ANTERIOR CERVICAL-LF, Medline Kit Number/SKU DYNJS3016.",
      "text": "The FDA logged enforcement record Z-2036-2026: Medline Industries, LP is voluntarily recalling Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows:   1. ANTERIOR CERVICAL FUSION PACK, Medline Kit Number/SKU DYNJ40566C;   2. OB PACK (OBSJD)642-LF, Medline Kit Number/SKU DYNJ47491F;   3. ANTERIOR CERVICAL-LF, Medline Kit Number/SKU DYNJ58274;   4. ANTERIOR CERVICAL-LF, Medline Kit Number/SKU DYNJ58344;   5. ANTERIOR CERVICAL-LF, Medline Kit Number/SKU DYNJS3016. — reason: During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.. Status: Ongoing — the recall is still being carried out.. Initiated 2026-03-19. Affected lots/codes: Medline Kit Number/SKU DYNJ40566C:  UDI/DI each10889942469659, UDI/DI case 40889942469650,  Lot Number: 22BBJ540;  Medline Kit Number/SKU DYNJ40566C:  UDI/DI each10889942469659, UDI/DI case 40889942469650,  Lot Number: 21LBM539;  Medline Kit Number/SKU DYNJ40566C:  UDI/DI each10889942469659, UDI/DI case 40889942469650,  Lot Number: 21IBX286;  Medline Kit Number/SKU DYNJ40566C:  UDI/DI each10889942469659, UDI/DI case 40889942469650,  Lot Number: 21HBM832;  Medline Kit Number/SKU DYNJ47491F:  UDI/DI each10193489586725, UDI/DI case 40193489586726,  Lot Number: 21KMD114;  Medline Kit Number/SKU DYNJ58274:  UDI/DI each10889942840724, UDI/DI case 40889942840725,  Lot Number: 22FMI371;  Medline Kit Number/SKU DYNJ58274:  UDI/DI each10889942840724, UDI/DI case 40889942840725,  Lot Number: 21IMD775;  Medline Kit Number/SKU DYNJ58344:  UDI/DI each10889942841721, UDI/DI case 40889942841722,  Lot Number: 23JBD782;  Medline Kit Number/SKU DYNJ58344:  UDI/DI each10889942841721, UDI/DI case 40889942841722,  Lot Number: 23HBY508;  Medline Kit Number/SKU DYNJ58344:  UDI/DI each10889942841721, UDI/DI case 40889942841722,  Lot Number: 23GBQ615;  Medline Kit Number/SKU DYNJ58344:  UDI/DI each10889942841721, UDI/DI case 40889942841722,  Lot Number: 23EBR984;  Medline Kit Number/SKU DYNJ58344:  UDI/DI each10889942841721, UDI/DI case 40889942841722,  Lot Number: 23EBD017;  Medline Kit Number/SKU DYNJ58344:  UDI/DI each10889942841721, UDI/DI case 40889942841722,  Lot Number: 23BBO048;  Medline Kit Number/SKU DYNJ58344:  UDI/DI each10889942841721, UDI/DI case 40889942841722,  Lot Number: 22JBI096;  Medline Kit Number/SKU DYNJ58344:  UDI/DI each10889942841721, UDI/DI case 40889942841722,  Lot Number: 22FBA057;  Medline Kit Number/SKU DYNJ58344:  UDI/DI each10889942841721, UDI/DI case 40889942841722,  Lot Number: 22CBA050;  Medline Kit Number/SKU DYNJ58344:  UDI/DI each10889942841721, UDI/DI case 40889942841722,  Lot Number: 21IBG464;  Medline Kit Number/SKU DYNJ58344:  UDI/DI each10889942841721, UDI/DI case 40889942841722,  Lot Number: 21GBJ471;  Medline Kit Number/SKU DYNJ58344:  UDI/DI each10889942841721, UDI/DI case 40889942841722,  Lot Number: 21EBA373;  Medline Kit Number/SKU DYNJ58344:  UDI/DI each10889942841721, UDI/DI case 40889942841722,  Lot Number: 21DBG514;  Medline Kit Number/SKU DYNJ58344:  UDI/DI each10889942841721, UDI/DI case 40889942841722,  Lot Number: 21ABD741;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 23IBQ007;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 23GBM279;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 23EBT579;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 23DBT199;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 23CBP725;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 23CBH452;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 23ABR478;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 22JBU430;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 22IBM433;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 22GBW568;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 22EBG751;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 22DBT428;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 22DBE203;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 22NBF066;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 21KBZ291;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 21IBL547;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 21FBQ973;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 21DBI879;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 26ABQ626;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 25KBI185;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 25JBK909;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 25HBN871;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 25FBI730;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 25DBR613;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 25BBP811;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 24KBT890;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 24HBT785;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 24HBH475;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 24FBP481;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 24DBH874;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 24CBG680;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 23LBI949.. 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-2036-2026&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-2036-2026&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-2036-2026/fda-classification",
      "@type": "schema:Claim",
      "name": "FDA classified recall Z-2036-2026 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-2036-2026&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-2036-2026&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-2036-2026/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": [
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      "@type": "schema:ItemList",
      "name": "FDA recall details — Z-2036-2026",
      "numberOfItems": 9,
      "itemListElement": [
        {
          "@type": "schema:ListItem",
          "position": 1,
          "item": {
            "Field": "Recall number",
            "Value": "Z-2036-2026",
            "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": "Medline Industries, LP",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 6,
          "item": {
            "Field": "Reason",
            "Value": "During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 7,
          "item": {
            "Field": "Initiated",
            "Value": "2026-03-19",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 8,
          "item": {
            "Field": "Lot/code info",
            "Value": "Medline Kit Number/SKU DYNJ40566C:  UDI/DI each10889942469659, UDI/DI case 40889942469650,  Lot Number: 22BBJ540;  Medline Kit Number/SKU DYNJ40566C:  UDI/DI each10889942469659, UDI/DI case 40889942469650,  Lot Number: 21LBM539;  Medline Kit Number/SKU DYNJ40566C:  UDI/DI each10889942469659, UDI/DI case 40889942469650,  Lot Number: 21IBX286;  Medline Kit Number/SKU DYNJ40566C:  UDI/DI each10889942469659, UDI/DI case 40889942469650,  Lot Number: 21HBM832;  Medline Kit Number/SKU DYNJ47491F:  UDI/DI each10193489586725, UDI/DI case 40193489586726,  Lot Number: 21KMD114;  Medline Kit Number/SKU DYNJ58274:  UDI/DI each10889942840724, UDI/DI case 40889942840725,  Lot Number: 22FMI371;  Medline Kit Number/SKU DYNJ58274:  UDI/DI each10889942840724, UDI/DI case 40889942840725,  Lot Number: 21IMD775;  Medline Kit Number/SKU DYNJ58344:  UDI/DI each10889942841721, UDI/DI case 40889942841722,  Lot Number: 23JBD782;  Medline Kit Number/SKU DYNJ58344:  UDI/DI each10889942841721, UDI/DI case 40889942841722,  Lot Number: 23HBY508;  Medline Kit Number/SKU DYNJ58344:  UDI/DI each10889942841721, UDI/DI case 40889942841722,  Lot Number: 23GBQ615;  Medline Kit Number/SKU DYNJ58344:  UDI/DI each10889942841721, UDI/DI case 40889942841722,  Lot Number: 23EBR984;  Medline Kit Number/SKU DYNJ58344:  UDI/DI each10889942841721, UDI/DI case 40889942841722,  Lot Number: 23EBD017;  Medline Kit Number/SKU DYNJ58344:  UDI/DI each10889942841721, UDI/DI case 40889942841722,  Lot Number: 23BBO048;  Medline Kit Number/SKU DYNJ58344:  UDI/DI each10889942841721, UDI/DI case 40889942841722,  Lot Number: 22JBI096;  Medline Kit Number/SKU DYNJ58344:  UDI/DI each10889942841721, UDI/DI case 40889942841722,  Lot Number: 22FBA057;  Medline Kit Number/SKU DYNJ58344:  UDI/DI each10889942841721, UDI/DI case 40889942841722,  Lot Number: 22CBA050;  Medline Kit Number/SKU DYNJ58344:  UDI/DI each10889942841721, UDI/DI case 40889942841722,  Lot Number: 21IBG464;  Medline Kit Number/SKU DYNJ58344:  UDI/DI each10889942841721, UDI/DI case 40889942841722,  Lot Number: 21GBJ471;  Medline Kit Number/SKU DYNJ58344:  UDI/DI each10889942841721, UDI/DI case 40889942841722,  Lot Number: 21EBA373;  Medline Kit Number/SKU DYNJ58344:  UDI/DI each10889942841721, UDI/DI case 40889942841722,  Lot Number: 21DBG514;  Medline Kit Number/SKU DYNJ58344:  UDI/DI each10889942841721, UDI/DI case 40889942841722,  Lot Number: 21ABD741;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 23IBQ007;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 23GBM279;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 23EBT579;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 23DBT199;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 23CBP725;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 23CBH452;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 23ABR478;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 22JBU430;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 22IBM433;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 22GBW568;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 22EBG751;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 22DBT428;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 22DBE203;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 22NBF066;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 21KBZ291;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 21IBL547;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 21FBQ973;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 21DBI879;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 26ABQ626;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 25KBI185;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 25JBK909;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 25HBN871;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 25FBI730;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 25DBR613;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 25BBP811;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 24KBT890;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 24HBT785;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 24HBH475;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 24FBP481;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 24DBH874;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 24CBG680;  Medline Kit Number/SKU DYNJS3016:  UDI/DI each10884389201640, UDI/DI case 40884389201641,  Lot Number: 23LBI949.",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 9,
          "item": {
            "Field": "Distribution pattern",
            "Value": "Worldwide distribution.",
            "Status": "recorded"
          }
        }
      ]
    }
  ]
}