{
  "@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-1055-2026.jsonld",
  "@type": "schema:Dataset",
  "name": "Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as:    1) DRAWER 2 IV SUPPLIES, Medline kit SKU ACC010271B;   2) DRAWER 2 IV FLUIDS & TUBING, Medline kit SKU ACC010416B;   3) OXYGENATION & TUBING TRAY, Medline kit SKU ACC010525C;   4) TOP DRAWER #6, Medline kit SKU ACC010688;   5) RRMC CODE CART DRAWER 3, Medline kit SKU ACC010770;   6) SURGERY BAG, Medline kit SKU DYKM1279C;   7) ADMISSION KIT, Medline kit SKU DYKS1179;   8) PRE OP KIT, Medline kit SKU DYKS1192C;   9) MEDLINE PEDIATRIC PATIENT PACK, Medline kit SKU DYKS1199B;   10) MEDLINE ADULT PATIENT PACKAGE, Medline kit SKU DYKS1200B;   11) GERMANTOWN PRE OP KIT, Medline kit SKU DYKS1248;   12) GERMANTOWN PRE OP BLOCK KIT, Medline kit SKU DYKS1249;   13) PRE OP KIT, Medline kit SKU DYKS1274A;   14) CATH LAB PRE OP START KIT, Medline kit SKU DYKS1324;   15) PRE OP KIT, Medline kit SKU DYKS1376;   16) PTC KIT, Medline kit SKU DYNDH1161A;   17) DR BROWN BODY, Medline kit SKU DYNJ910487.",
  "description": "FDA recall Z-1055-2026 — Medline Industries, LP is recalling Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as:    1) DRAWER 2 IV SUPPLIES, Medline kit SKU ACC010271B;   2) DRAWER 2 IV FLUIDS & TUBING, Medline kit SKU ACC010416B;   3) OXYGENATION & TUBING TRAY, Medline kit SKU ACC010525C;   4) TOP DRAWER #6, Medline kit SKU ACC010688;   5) RRMC CODE CART DRAWER 3, Medline kit SKU ACC010770;   6) SURGERY BAG, Medline kit SKU DYKM1279C;   7) ADMISSION KIT, Medline kit SKU DYKS1179;   8) PRE OP KIT, Medline kit SKU DYKS1192C;   9) MEDLINE PEDIATRIC PATIENT PACK, Medline kit SKU DYKS1199B;   10) MEDLINE ADULT PATIENT PACKAGE, Medline kit SKU DYKS1200B;   11) GERMANTOWN PRE OP KIT, Medline kit SKU DYKS1248;   12) GERMANTOWN PRE OP BLOCK KIT, Medline kit SKU DYKS1249;   13) PRE OP KIT, Medline kit SKU DYKS1274A;   14) CATH LAB PRE OP START KIT, Medline kit SKU DYKS1324;   15) PRE OP KIT, Medline kit SKU DYKS1376;   16) PTC KIT, Medline kit SKU DYNDH1161A;   17) DR BROWN BODY, Medline kit SKU DYNJ910487. (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-1055-2026&lang=eng",
  "about": {
    "@type": "schema:MedicalDevice",
    "name": "Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as:    1) DRAWER 2 IV SUPPLIES, Medline kit SKU ACC010271B;   2) DRAWER 2 IV FLUIDS & TUBING, Medline kit SKU ACC010416B;   3) OXYGENATION & TUBING TRAY, Medline kit SKU ACC010525C;   4) TOP DRAWER #6, Medline kit SKU ACC010688;   5) RRMC CODE CART DRAWER 3, Medline kit SKU ACC010770;   6) SURGERY BAG, Medline kit SKU DYKM1279C;   7) ADMISSION KIT, Medline kit SKU DYKS1179;   8) PRE OP KIT, Medline kit SKU DYKS1192C;   9) MEDLINE PEDIATRIC PATIENT PACK, Medline kit SKU DYKS1199B;   10) MEDLINE ADULT PATIENT PACKAGE, Medline kit SKU DYKS1200B;   11) GERMANTOWN PRE OP KIT, Medline kit SKU DYKS1248;   12) GERMANTOWN PRE OP BLOCK KIT, Medline kit SKU DYKS1249;   13) PRE OP KIT, Medline kit SKU DYKS1274A;   14) CATH LAB PRE OP START KIT, Medline kit SKU DYKS1324;   15) PRE OP KIT, Medline kit SKU DYKS1376;   16) PTC KIT, Medline kit SKU DYNDH1161A;   17) DR BROWN BODY, Medline kit SKU DYNJ910487.",
    "manufacturer": {
      "@type": "schema:Organization",
      "name": "Medline Industries, LP"
    }
  },
  "claims": [
    {
      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-1055-2026/enforcement-record",
      "@type": "schema:Claim",
      "name": "FDA recall Z-1055-2026: Medline Industries, LP is recalling Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as:    1) DRAWER 2 IV SUPPLIES, Medline kit SKU ACC010271B;   2) DRAWER 2 IV FLUIDS & TUBING, Medline kit SKU ACC010416B;   3) OXYGENATION & TUBING TRAY, Medline kit SKU ACC010525C;   4) TOP DRAWER #6, Medline kit SKU ACC010688;   5) RRMC CODE CART DRAWER 3, Medline kit SKU ACC010770;   6) SURGERY BAG, Medline kit SKU DYKM1279C;   7) ADMISSION KIT, Medline kit SKU DYKS1179;   8) PRE OP KIT, Medline kit SKU DYKS1192C;   9) MEDLINE PEDIATRIC PATIENT PACK, Medline kit SKU DYKS1199B;   10) MEDLINE ADULT PATIENT PACKAGE, Medline kit SKU DYKS1200B;   11) GERMANTOWN PRE OP KIT, Medline kit SKU DYKS1248;   12) GERMANTOWN PRE OP BLOCK KIT, Medline kit SKU DYKS1249;   13) PRE OP KIT, Medline kit SKU DYKS1274A;   14) CATH LAB PRE OP START KIT, Medline kit SKU DYKS1324;   15) PRE OP KIT, Medline kit SKU DYKS1376;   16) PTC KIT, Medline kit SKU DYNDH1161A;   17) DR BROWN BODY, Medline kit SKU DYNJ910487.",
      "text": "The FDA logged enforcement record Z-1055-2026: Medline Industries, LP is voluntarily recalling Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as:    1) DRAWER 2 IV SUPPLIES, Medline kit SKU ACC010271B;   2) DRAWER 2 IV FLUIDS & TUBING, Medline kit SKU ACC010416B;   3) OXYGENATION & TUBING TRAY, Medline kit SKU ACC010525C;   4) TOP DRAWER #6, Medline kit SKU ACC010688;   5) RRMC CODE CART DRAWER 3, Medline kit SKU ACC010770;   6) SURGERY BAG, Medline kit SKU DYKM1279C;   7) ADMISSION KIT, Medline kit SKU DYKS1179;   8) PRE OP KIT, Medline kit SKU DYKS1192C;   9) MEDLINE PEDIATRIC PATIENT PACK, Medline kit SKU DYKS1199B;   10) MEDLINE ADULT PATIENT PACKAGE, Medline kit SKU DYKS1200B;   11) GERMANTOWN PRE OP KIT, Medline kit SKU DYKS1248;   12) GERMANTOWN PRE OP BLOCK KIT, Medline kit SKU DYKS1249;   13) PRE OP KIT, Medline kit SKU DYKS1274A;   14) CATH LAB PRE OP START KIT, Medline kit SKU DYKS1324;   15) PRE OP KIT, Medline kit SKU DYKS1376;   16) PTC KIT, Medline kit SKU DYNDH1161A;   17) DR BROWN BODY, Medline kit SKU DYNJ910487. — reason: Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions.. Status: Ongoing — the recall is still being carried out.. Initiated 2025-11-26. Affected lots/codes: Medline kit SKU ACC010271B, UDI/DI 10193489484953 (EA) 40193489484954 (CS), Lot number 25IDB125;  Medline kit SKU ACC010271B, UDI/DI 10193489484953 (EA) 40193489484954 (CS), Lot number 25IDB400;  Medline kit SKU ACC010271B, UDI/DI 10193489484953 (EA) 40193489484954 (CS), Lot number 25JDB835;  Medline kit SKU ACC010271B, UDI/DI 10193489484953 (EA) 40193489484954 (CS), Lot number 25KDA036;  Medline kit SKU ACC010271B, UDI/DI 10193489484953 (EA) 40193489484954 (CS), Lot number 25KDA248;  Medline kit SKU ACC010416B, UDI/DI 10195327223670 (EA) 40195327223671 (CS), Lot number 25IDA545;  Medline kit SKU ACC010416B, UDI/DI 10195327223670 (EA) 40195327223671 (CS), Lot number 25JDB867;  Medline kit SKU ACC010525C, UDI/DI 10198459027765 (EA) 40198459027766 (CS), Lot number 25KDA768;  Medline kit SKU ACC010688, UDI/DI 10195327432713 (EA) 40195327432714 (CS), Lot number 25HDB656;  Medline kit SKU ACC010688, UDI/DI 10195327432713 (EA) 40195327432714 (CS), Lot number 25IDA638;  Medline kit SKU ACC010688, UDI/DI 10195327432713 (EA) 40195327432714 (CS), Lot number 25JDA666;  Medline kit SKU ACC010770, UDI/DI 10195327576998 (EA) 40195327576999 (CS), Lot number 25HDA878;  Medline kit SKU ACC010770, UDI/DI 10195327576998 (EA) 40195327576999 (CS), Lot number 25IDA087;  Medline kit SKU ACC010770, UDI/DI 10195327576998 (EA) 40195327576999 (CS), Lot number 25IDA817;  Medline kit SKU ACC010770, UDI/DI 10195327576998 (EA) 40195327576999 (CS), Lot number 25JDB317;  Medline kit SKU DYKM1279C, UDI/DI 10889942519583 (EA) 40889942519584 (CS), Lot number 25IBL412;  Medline kit SKU DYKM1279C, UDI/DI 10889942519583 (EA) 40889942519584 (CS), Lot number 25KBK165;  Medline kit SKU DYKS1179, UDI/DI 10193489711981 (EA) 40193489711982 (CS), Lot number 25IMD671;  Medline kit SKU DYKS1179, UDI/DI 10193489711981 (EA) 40193489711982 (CS), Lot number 25JMG868;  Medline kit SKU DYKS1192C, UDI/DI 10193489849707 (EA) 40193489849708 (CS), Lot number 25KME757;  Medline kit SKU DYKS1199B, UDI/DI 10193489403831 (EA) 40193489403832 (CS), Lot number 25HBF059;  Medline kit SKU DYKS1199B, UDI/DI 10193489403831 (EA) 40193489403832 (CS), Lot number 25JBU391;  Medline kit SKU DYKS1200B, UDI/DI 10193489235425 (EA) 40193489235426 (CS), Lot number 25IBT744;  Medline kit SKU DYKS1200B, UDI/DI 10193489235425 (EA) 40193489235426 (CS), Lot number 25KBG976;  Medline kit SKU DYKS1248, UDI/DI 10193489305708 (EA) 40193489305709 (CS), Lot number 25JBS281;  Medline kit SKU DYKS1249, UDI/DI 10193489305715 (EA) 40193489305716 (CS), Lot number 25HBJ008;  Medline kit SKU DYKS1249, UDI/DI 10193489305715 (EA) 40193489305716 (CS), Lot number 25HBV936;  Medline kit SKU DYKS1249, UDI/DI 10193489305715 (EA) 40193489305716 (CS), Lot number 25IBB540;  Medline kit SKU DYKS1274A, UDI/DI 10195327058890 (EA) 40195327058891 (CS), Lot number 25HBF086;  Medline kit SKU DYKS1274A, UDI/DI 10195327058890 (EA) 40195327058891 (CS), Lot number 25IBF923;  Medline kit SKU DYKS1324, UDI/DI 10193489969962 (EA) 40193489969963 (CS), Lot number 25IBR790;  Medline kit SKU DYKS1376, UDI/DI 10195327216498 (EA) 40195327216499 (CS), Lot number 25HBF087;  Medline kit SKU DYKS1376, UDI/DI 10195327216498 (EA) 40195327216499 (CS), Lot number 25IBS865;  Medline kit SKU DYNDH1161A, UDI/DI 10889942731299 (EA) 40889942731290 (CS), Lot number 25HBG750;  Medline kit SKU DYNJ910487, UDI/DI 10198459004841 (EA) 40198459004842 (CS), Lot number 25GMK728;  Medline kit SKU DYNJ910487, UDI/DI 10198459004841 (EA) 40198459004842 (CS), Lot number 25HMI417;. 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-1055-2026&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-1055-2026&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-1055-2026/fda-classification",
      "@type": "schema:Claim",
      "name": "FDA classified recall Z-1055-2026 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-1055-2026&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-1055-2026&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-1055-2026/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": [
    {
      "@type": "schema:ItemList",
      "name": "FDA recall details — Z-1055-2026",
      "numberOfItems": 9,
      "itemListElement": [
        {
          "@type": "schema:ListItem",
          "position": 1,
          "item": {
            "Field": "Recall number",
            "Value": "Z-1055-2026",
            "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": "Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions.",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 7,
          "item": {
            "Field": "Initiated",
            "Value": "2025-11-26",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 8,
          "item": {
            "Field": "Lot/code info",
            "Value": "Medline kit SKU ACC010271B, UDI/DI 10193489484953 (EA) 40193489484954 (CS), Lot number 25IDB125;  Medline kit SKU ACC010271B, UDI/DI 10193489484953 (EA) 40193489484954 (CS), Lot number 25IDB400;  Medline kit SKU ACC010271B, UDI/DI 10193489484953 (EA) 40193489484954 (CS), Lot number 25JDB835;  Medline kit SKU ACC010271B, UDI/DI 10193489484953 (EA) 40193489484954 (CS), Lot number 25KDA036;  Medline kit SKU ACC010271B, UDI/DI 10193489484953 (EA) 40193489484954 (CS), Lot number 25KDA248;  Medline kit SKU ACC010416B, UDI/DI 10195327223670 (EA) 40195327223671 (CS), Lot number 25IDA545;  Medline kit SKU ACC010416B, UDI/DI 10195327223670 (EA) 40195327223671 (CS), Lot number 25JDB867;  Medline kit SKU ACC010525C, UDI/DI 10198459027765 (EA) 40198459027766 (CS), Lot number 25KDA768;  Medline kit SKU ACC010688, UDI/DI 10195327432713 (EA) 40195327432714 (CS), Lot number 25HDB656;  Medline kit SKU ACC010688, UDI/DI 10195327432713 (EA) 40195327432714 (CS), Lot number 25IDA638;  Medline kit SKU ACC010688, UDI/DI 10195327432713 (EA) 40195327432714 (CS), Lot number 25JDA666;  Medline kit SKU ACC010770, UDI/DI 10195327576998 (EA) 40195327576999 (CS), Lot number 25HDA878;  Medline kit SKU ACC010770, UDI/DI 10195327576998 (EA) 40195327576999 (CS), Lot number 25IDA087;  Medline kit SKU ACC010770, UDI/DI 10195327576998 (EA) 40195327576999 (CS), Lot number 25IDA817;  Medline kit SKU ACC010770, UDI/DI 10195327576998 (EA) 40195327576999 (CS), Lot number 25JDB317;  Medline kit SKU DYKM1279C, UDI/DI 10889942519583 (EA) 40889942519584 (CS), Lot number 25IBL412;  Medline kit SKU DYKM1279C, UDI/DI 10889942519583 (EA) 40889942519584 (CS), Lot number 25KBK165;  Medline kit SKU DYKS1179, UDI/DI 10193489711981 (EA) 40193489711982 (CS), Lot number 25IMD671;  Medline kit SKU DYKS1179, UDI/DI 10193489711981 (EA) 40193489711982 (CS), Lot number 25JMG868;  Medline kit SKU DYKS1192C, UDI/DI 10193489849707 (EA) 40193489849708 (CS), Lot number 25KME757;  Medline kit SKU DYKS1199B, UDI/DI 10193489403831 (EA) 40193489403832 (CS), Lot number 25HBF059;  Medline kit SKU DYKS1199B, UDI/DI 10193489403831 (EA) 40193489403832 (CS), Lot number 25JBU391;  Medline kit SKU DYKS1200B, UDI/DI 10193489235425 (EA) 40193489235426 (CS), Lot number 25IBT744;  Medline kit SKU DYKS1200B, UDI/DI 10193489235425 (EA) 40193489235426 (CS), Lot number 25KBG976;  Medline kit SKU DYKS1248, UDI/DI 10193489305708 (EA) 40193489305709 (CS), Lot number 25JBS281;  Medline kit SKU DYKS1249, UDI/DI 10193489305715 (EA) 40193489305716 (CS), Lot number 25HBJ008;  Medline kit SKU DYKS1249, UDI/DI 10193489305715 (EA) 40193489305716 (CS), Lot number 25HBV936;  Medline kit SKU DYKS1249, UDI/DI 10193489305715 (EA) 40193489305716 (CS), Lot number 25IBB540;  Medline kit SKU DYKS1274A, UDI/DI 10195327058890 (EA) 40195327058891 (CS), Lot number 25HBF086;  Medline kit SKU DYKS1274A, UDI/DI 10195327058890 (EA) 40195327058891 (CS), Lot number 25IBF923;  Medline kit SKU DYKS1324, UDI/DI 10193489969962 (EA) 40193489969963 (CS), Lot number 25IBR790;  Medline kit SKU DYKS1376, UDI/DI 10195327216498 (EA) 40195327216499 (CS), Lot number 25HBF087;  Medline kit SKU DYKS1376, UDI/DI 10195327216498 (EA) 40195327216499 (CS), Lot number 25IBS865;  Medline kit SKU DYNDH1161A, UDI/DI 10889942731299 (EA) 40889942731290 (CS), Lot number 25HBG750;  Medline kit SKU DYNJ910487, UDI/DI 10198459004841 (EA) 40198459004842 (CS), Lot number 25GMK728;  Medline kit SKU DYNJ910487, UDI/DI 10198459004841 (EA) 40198459004842 (CS), Lot number 25HMI417;",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 9,
          "item": {
            "Field": "Distribution pattern",
            "Value": "US Nationwide distribution.",
            "Status": "recorded"
          }
        }
      ]
    }
  ]
}