{
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  "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-1102-2024.jsonld",
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  "name": "MEDLINE Kits, trays, and packs labeled as follows:    a)\tASC GENERAL MINOR CDS, REF CDS983673G;   b)\tASC GENERAL MINOR CDS, REF CDS983673I;   c)\tC NURSE BAG KIT, REF DYKM1425;   d)\tDAILY DRIVELINE MGMT KIT w/PER, REF DT18700;   e)\tGASTRIC CULTURE PACK, REF DYNJ53966A;   f)\tGASTRIC CULTURE PACK, REF DYNJ53966AH;   g)\tHERNIA, REF CDS982034R;   h)\tHERNIA, REF CDS982034S;   i)\tHERNIA PACK, REF DYNJ39331B;   j)\tLAP APPY PACK, REF DYNJ37709J;   k)\tLAP CHOLE CDS, REF CDS983912V;   l)\tLAP CHOLE CDS, REF CDS983912W;   m)\tLAP CHOLE CDS, REF CDS983912X;   n)\tLAP CHOLE CDS, REF CDS983912Y;   o)\tLAPAROSCOPY PACK, REF DYNJ41417J;   p)\tLAPAROTOMY CDS-LF, REF CDS860091A;   q)\tLOWER EXTREMITY, REF DYNJ46222M;   r)\tMAJOR PACK, REF DYNJ80578A;   s)\tMINOR PACK, REF DYNJ67217D;   t)\tN L MINOR CDS, REF CDS982518O;   u)\tN L MINOR CDS, REF CDS982518P;   v)\tNON STERILE I&D KIT, REF DYKM1438;   w)\tPACK,GU MINOR, REF DYNJ906885B;   x)\tPLASTICS SUTURE TRAY, REF SUT13535;   y)\tRESPIRATORY KIT, REF DYKM1404;   z)\tTRACH CARE TRAY, REF DYNDJ1057A;",
  "description": "FDA recall Z-1102-2024 — MEDLINE INDUSTRIES, LP - Northfield is recalling MEDLINE Kits, trays, and packs labeled as follows:    a)\tASC GENERAL MINOR CDS, REF CDS983673G;   b)\tASC GENERAL MINOR CDS, REF CDS983673I;   c)\tC NURSE BAG KIT, REF DYKM1425;   d)\tDAILY DRIVELINE MGMT KIT w/PER, REF DT18700;   e)\tGASTRIC CULTURE PACK, REF DYNJ53966A;   f)\tGASTRIC CULTURE PACK, REF DYNJ53966AH;   g)\tHERNIA, REF CDS982034R;   h)\tHERNIA, REF CDS982034S;   i)\tHERNIA PACK, REF DYNJ39331B;   j)\tLAP APPY PACK, REF DYNJ37709J;   k)\tLAP CHOLE CDS, REF CDS983912V;   l)\tLAP CHOLE CDS, REF CDS983912W;   m)\tLAP CHOLE CDS, REF CDS983912X;   n)\tLAP CHOLE CDS, REF CDS983912Y;   o)\tLAPAROSCOPY PACK, REF DYNJ41417J;   p)\tLAPAROTOMY CDS-LF, REF CDS860091A;   q)\tLOWER EXTREMITY, REF DYNJ46222M;   r)\tMAJOR PACK, REF DYNJ80578A;   s)\tMINOR PACK, REF DYNJ67217D;   t)\tN L MINOR CDS, REF CDS982518O;   u)\tN L MINOR CDS, REF CDS982518P;   v)\tNON STERILE I&D KIT, REF DYKM1438;   w)\tPACK,GU MINOR, REF DYNJ906885B;   x)\tPLASTICS SUTURE TRAY, REF SUT13535;   y)\tRESPIRATORY KIT, REF DYKM1404;   z)\tTRACH CARE TRAY, REF DYNDJ1057A; (Devices, Class I). 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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  "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"
    }
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  "sameAs": "https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=Z-1102-2024&lang=eng",
  "about": {
    "@type": "schema:MedicalDevice",
    "name": "MEDLINE Kits, trays, and packs labeled as follows:    a)\tASC GENERAL MINOR CDS, REF CDS983673G;   b)\tASC GENERAL MINOR CDS, REF CDS983673I;   c)\tC NURSE BAG KIT, REF DYKM1425;   d)\tDAILY DRIVELINE MGMT KIT w/PER, REF DT18700;   e)\tGASTRIC CULTURE PACK, REF DYNJ53966A;   f)\tGASTRIC CULTURE PACK, REF DYNJ53966AH;   g)\tHERNIA, REF CDS982034R;   h)\tHERNIA, REF CDS982034S;   i)\tHERNIA PACK, REF DYNJ39331B;   j)\tLAP APPY PACK, REF DYNJ37709J;   k)\tLAP CHOLE CDS, REF CDS983912V;   l)\tLAP CHOLE CDS, REF CDS983912W;   m)\tLAP CHOLE CDS, REF CDS983912X;   n)\tLAP CHOLE CDS, REF CDS983912Y;   o)\tLAPAROSCOPY PACK, REF DYNJ41417J;   p)\tLAPAROTOMY CDS-LF, REF CDS860091A;   q)\tLOWER EXTREMITY, REF DYNJ46222M;   r)\tMAJOR PACK, REF DYNJ80578A;   s)\tMINOR PACK, REF DYNJ67217D;   t)\tN L MINOR CDS, REF CDS982518O;   u)\tN L MINOR CDS, REF CDS982518P;   v)\tNON STERILE I&D KIT, REF DYKM1438;   w)\tPACK,GU MINOR, REF DYNJ906885B;   x)\tPLASTICS SUTURE TRAY, REF SUT13535;   y)\tRESPIRATORY KIT, REF DYKM1404;   z)\tTRACH CARE TRAY, REF DYNDJ1057A;",
    "manufacturer": {
      "@type": "schema:Organization",
      "name": "MEDLINE INDUSTRIES, LP - Northfield"
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  "claims": [
    {
      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-1102-2024/enforcement-record",
      "@type": "schema:Claim",
      "name": "FDA recall Z-1102-2024: MEDLINE INDUSTRIES, LP - Northfield is recalling MEDLINE Kits, trays, and packs labeled as follows:    a)\tASC GENERAL MINOR CDS, REF CDS983673G;   b)\tASC GENERAL MINOR CDS, REF CDS983673I;   c)\tC NURSE BAG KIT, REF DYKM1425;   d)\tDAILY DRIVELINE MGMT KIT w/PER, REF DT18700;   e)\tGASTRIC CULTURE PACK, REF DYNJ53966A;   f)\tGASTRIC CULTURE PACK, REF DYNJ53966AH;   g)\tHERNIA, REF CDS982034R;   h)\tHERNIA, REF CDS982034S;   i)\tHERNIA PACK, REF DYNJ39331B;   j)\tLAP APPY PACK, REF DYNJ37709J;   k)\tLAP CHOLE CDS, REF CDS983912V;   l)\tLAP CHOLE CDS, REF CDS983912W;   m)\tLAP CHOLE CDS, REF CDS983912X;   n)\tLAP CHOLE CDS, REF CDS983912Y;   o)\tLAPAROSCOPY PACK, REF DYNJ41417J;   p)\tLAPAROTOMY CDS-LF, REF CDS860091A;   q)\tLOWER EXTREMITY, REF DYNJ46222M;   r)\tMAJOR PACK, REF DYNJ80578A;   s)\tMINOR PACK, REF DYNJ67217D;   t)\tN L MINOR CDS, REF CDS982518O;   u)\tN L MINOR CDS, REF CDS982518P;   v)\tNON STERILE I&D KIT, REF DYKM1438;   w)\tPACK,GU MINOR, REF DYNJ906885B;   x)\tPLASTICS SUTURE TRAY, REF SUT13535;   y)\tRESPIRATORY KIT, REF DYKM1404;   z)\tTRACH CARE TRAY, REF DYNDJ1057A;",
      "text": "The FDA logged enforcement record Z-1102-2024: MEDLINE INDUSTRIES, LP - Northfield is voluntarily recalling MEDLINE Kits, trays, and packs labeled as follows:    a)\tASC GENERAL MINOR CDS, REF CDS983673G;   b)\tASC GENERAL MINOR CDS, REF CDS983673I;   c)\tC NURSE BAG KIT, REF DYKM1425;   d)\tDAILY DRIVELINE MGMT KIT w/PER, REF DT18700;   e)\tGASTRIC CULTURE PACK, REF DYNJ53966A;   f)\tGASTRIC CULTURE PACK, REF DYNJ53966AH;   g)\tHERNIA, REF CDS982034R;   h)\tHERNIA, REF CDS982034S;   i)\tHERNIA PACK, REF DYNJ39331B;   j)\tLAP APPY PACK, REF DYNJ37709J;   k)\tLAP CHOLE CDS, REF CDS983912V;   l)\tLAP CHOLE CDS, REF CDS983912W;   m)\tLAP CHOLE CDS, REF CDS983912X;   n)\tLAP CHOLE CDS, REF CDS983912Y;   o)\tLAPAROSCOPY PACK, REF DYNJ41417J;   p)\tLAPAROTOMY CDS-LF, REF CDS860091A;   q)\tLOWER EXTREMITY, REF DYNJ46222M;   r)\tMAJOR PACK, REF DYNJ80578A;   s)\tMINOR PACK, REF DYNJ67217D;   t)\tN L MINOR CDS, REF CDS982518O;   u)\tN L MINOR CDS, REF CDS982518P;   v)\tNON STERILE I&D KIT, REF DYKM1438;   w)\tPACK,GU MINOR, REF DYNJ906885B;   x)\tPLASTICS SUTURE TRAY, REF SUT13535;   y)\tRESPIRATORY KIT, REF DYKM1404;   z)\tTRACH CARE TRAY, REF DYNDJ1057A; — reason: Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components):  0.9% Sodium Chloride Irrigation USP, Sterile Water for Irrigation USP and Saline Flush Syringe. Nurse Assist issued a recall due to the potential lack of sterility, which could result in the solution being non sterile.. Status: Ongoing — the recall is still being carried out.. Initiated 2023-11-15. Affected lots/codes: a) REF CDS983673G, UDI/DI 40193489951746 (case), 10193489951745 (unit), Lot Numbers: 22EDA378, 22EDB208;    b) REF CDS983673I, UDI/DI 40195327147335 (case), 10195327147334 (unit), Lot Numbers:  22GBJ096, 22GBJ097, 22HBR769, 22KBN934, 23ABH521, 23ABM586, 23BBR709, 23DBL344;     c) REF DYKM1425, UDI/DI 40889942511236 (case), 10889942511235 (unit), Lot Numbers:  22DLA695, 22FLA284, 22GLA016, 22ILA012, 22ILA463, 22KLA336, 23ALA341, 23BLA132, 23DLB048, 23ELA454, 23FLA774, 23HLA165, 23ILB030, 23JLA435;   d) REF DT18700, UDI/DI 653160275087 (case), 10653160275084 (unit), Lot Numbers:  23EBC489;   e) REF DYNJ53966A, UDI/DI 40889942964681 (case), 10889942964680 (unit), Lot Numbers: 23CMB869, 23DMG880, 23EMG449, 23FMC889, 23HMA233, 23IMD181;      f) REF DYNJ53966AH, UDI/DI 40889942964681 (case), 10889942964680 (unit), Lot Numbers:   23CMB869, 23DMG880, 23EMG449, 23FMC889, 23HMA233, 23IMD181,         g) REF CDS982034R, UDI/DI 40195327003740 (case), 10195327003739 (unit), Lot Numbers:  21LBB488, 21LBC635, 22HBW422;    h) REF CDS982034S, UDI/DI 40195327295364 (case), 10195327295363(unit), Lot Numbers:  23ABB710, 23BBA114, 23EBB482;   i) REF DYNJ39331B, UDI/DI 40889942731580 (case), 10889942731589 (unit), Lot Numbers:  22HBH194, 22JBE708, 22LBL321, 23GBV891, 23IBA384;   j) REF DYNJ37709J, UDI/DI 40193489376075 (case), 10193489376074 (unit), Lot Numbers:  22FMG179;   k) REF CDS983912V, UDI/DI 40195327057146 (case), 10195327057145 (unit), Lot Numbers:  22BBX974, 22DBG451, 22DBO438, 22FBM809;   l) REF CDS983912W, UDI/DI 40195327238408 (case), 10195327238407 (unit), Lot Numbers:  22KBI248, 23CBC518, 23DBM244;   m) REF CDS983912X, UDI/DI 40195327403141 (case), 10195327403140 (unit), Lot Numbers:  23EBK644;   n) REF CDS983912Y, UDI/DI 40195327417827 (case), 10195327417826 (unit), Lot Numbers:  23FBS625, 23HBD741, 23HBO315, 23IBC397, 23IBM310;   o) REF DYNJ41417J, UDI/DI 40195327220991 (case), 10195327220990 (unit), Lot Numbers:  23FBQ267;   p) REF CDS860091A, UDI/DI 40884389018324 (case), 10884389018323 (unit), Lot Numbers:  22ABW443, 22CBU907, 22FMA320, 22GMH940, 22IMI179, 22KMA029, 23AMJ550, 23CMF095, 23FMI870, 23GMF353;   q) REF DYNJ46222M, UDI/DI 40195327437566 (case), 10195327437565 (unit), Lot Numbers:  23GBP791;   r) REF DYNJ80578A, UDI/DI 40195327063819 (case), 10195327063818 (unit), Lot Numbers:  22FBO880;   s) REF DYNJ67217D, UDI/DI 40195327278022 (case), 10195327278021 (unit), Lot Numbers:  23DBC699, 23EBB789, 23GBC854, 23GBP633;   t) REF CDS982518O, UDI/DI 40195327247387 (case), 10195327247386 (unit), Lot Numbers:  23ABD137;   u) REF CDS982518P, UDI/DI 40195327318858 (case), 10195327318857 (unit), Lot Numbers:  23BBM210;   v) REF DYKM1438, UDI/DI 40889942529965 (case), 10889942529964 (unit), Lot Numbers:   22DDB583, 22FDA732, 22HDA409, 22JDA278, 22LDA778, 23BDB559, 23FDC186, 23IDA954;   w) REF DYNJ906885B, UDI/DI 40193489972543 (case), 10193489972542 (unit), Lot Numbers:  22GBF087;   x) REF SUT13535, UDI/DI 40193489440271 (case), 10193489440270 (case), Lot Numbers:   23GBD750;   y) REF DYKM1404, UDI/DI 40889942473831 (case), 10889942473830 (unit), Lot Numbers:   22JBQ565, 23CBG138, 23EBO035, 23EBW986, 23GBP589;   z) REF DYNDJ1057A, UDI/DI 40888277204790 (case), 10888277204799 (unit), Lot Numbers:  23DBC974. 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-1102-2024&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-1102-2024&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-1102-2024/fda-classification",
      "@type": "schema:Claim",
      "name": "FDA classified recall Z-1102-2024 as Class I",
      "text": "The FDA assigned this recall Class I: Class I — the FDA judged there is a reasonable probability that use of the product would cause serious harm or death.. 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-1102-2024&lang=eng",
        "value": "Class I",
        "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-1102-2024&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-1102-2024/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-1102-2024",
      "numberOfItems": 9,
      "itemListElement": [
        {
          "@type": "schema:ListItem",
          "position": 1,
          "item": {
            "Field": "Recall number",
            "Value": "Z-1102-2024",
            "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 I",
            "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 - Northfield",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 6,
          "item": {
            "Field": "Reason",
            "Value": "Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components):  0.9% Sodium Chloride Irrigation USP, Sterile Water for Irrigation USP and Saline Flush Syringe. Nurse Assist issued a recall due to the potential lack of sterility, which could result in the solution being non sterile.",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 7,
          "item": {
            "Field": "Initiated",
            "Value": "2023-11-15",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 8,
          "item": {
            "Field": "Lot/code info",
            "Value": "a) REF CDS983673G, UDI/DI 40193489951746 (case), 10193489951745 (unit), Lot Numbers: 22EDA378, 22EDB208;    b) REF CDS983673I, UDI/DI 40195327147335 (case), 10195327147334 (unit), Lot Numbers:  22GBJ096, 22GBJ097, 22HBR769, 22KBN934, 23ABH521, 23ABM586, 23BBR709, 23DBL344;     c) REF DYKM1425, UDI/DI 40889942511236 (case), 10889942511235 (unit), Lot Numbers:  22DLA695, 22FLA284, 22GLA016, 22ILA012, 22ILA463, 22KLA336, 23ALA341, 23BLA132, 23DLB048, 23ELA454, 23FLA774, 23HLA165, 23ILB030, 23JLA435;   d) REF DT18700, UDI/DI 653160275087 (case), 10653160275084 (unit), Lot Numbers:  23EBC489;   e) REF DYNJ53966A, UDI/DI 40889942964681 (case), 10889942964680 (unit), Lot Numbers: 23CMB869, 23DMG880, 23EMG449, 23FMC889, 23HMA233, 23IMD181;      f) REF DYNJ53966AH, UDI/DI 40889942964681 (case), 10889942964680 (unit), Lot Numbers:   23CMB869, 23DMG880, 23EMG449, 23FMC889, 23HMA233, 23IMD181,         g) REF CDS982034R, UDI/DI 40195327003740 (case), 10195327003739 (unit), Lot Numbers:  21LBB488, 21LBC635, 22HBW422;    h) REF CDS982034S, UDI/DI 40195327295364 (case), 10195327295363(unit), Lot Numbers:  23ABB710, 23BBA114, 23EBB482;   i) REF DYNJ39331B, UDI/DI 40889942731580 (case), 10889942731589 (unit), Lot Numbers:  22HBH194, 22JBE708, 22LBL321, 23GBV891, 23IBA384;   j) REF DYNJ37709J, UDI/DI 40193489376075 (case), 10193489376074 (unit), Lot Numbers:  22FMG179;   k) REF CDS983912V, UDI/DI 40195327057146 (case), 10195327057145 (unit), Lot Numbers:  22BBX974, 22DBG451, 22DBO438, 22FBM809;   l) REF CDS983912W, UDI/DI 40195327238408 (case), 10195327238407 (unit), Lot Numbers:  22KBI248, 23CBC518, 23DBM244;   m) REF CDS983912X, UDI/DI 40195327403141 (case), 10195327403140 (unit), Lot Numbers:  23EBK644;   n) REF CDS983912Y, UDI/DI 40195327417827 (case), 10195327417826 (unit), Lot Numbers:  23FBS625, 23HBD741, 23HBO315, 23IBC397, 23IBM310;   o) REF DYNJ41417J, UDI/DI 40195327220991 (case), 10195327220990 (unit), Lot Numbers:  23FBQ267;   p) REF CDS860091A, UDI/DI 40884389018324 (case), 10884389018323 (unit), Lot Numbers:  22ABW443, 22CBU907, 22FMA320, 22GMH940, 22IMI179, 22KMA029, 23AMJ550, 23CMF095, 23FMI870, 23GMF353;   q) REF DYNJ46222M, UDI/DI 40195327437566 (case), 10195327437565 (unit), Lot Numbers:  23GBP791;   r) REF DYNJ80578A, UDI/DI 40195327063819 (case), 10195327063818 (unit), Lot Numbers:  22FBO880;   s) REF DYNJ67217D, UDI/DI 40195327278022 (case), 10195327278021 (unit), Lot Numbers:  23DBC699, 23EBB789, 23GBC854, 23GBP633;   t) REF CDS982518O, UDI/DI 40195327247387 (case), 10195327247386 (unit), Lot Numbers:  23ABD137;   u) REF CDS982518P, UDI/DI 40195327318858 (case), 10195327318857 (unit), Lot Numbers:  23BBM210;   v) REF DYKM1438, UDI/DI 40889942529965 (case), 10889942529964 (unit), Lot Numbers:   22DDB583, 22FDA732, 22HDA409, 22JDA278, 22LDA778, 23BDB559, 23FDC186, 23IDA954;   w) REF DYNJ906885B, UDI/DI 40193489972543 (case), 10193489972542 (unit), Lot Numbers:  22GBF087;   x) REF SUT13535, UDI/DI 40193489440271 (case), 10193489440270 (case), Lot Numbers:   23GBD750;   y) REF DYKM1404, UDI/DI 40889942473831 (case), 10889942473830 (unit), Lot Numbers:   22JBQ565, 23CBG138, 23EBO035, 23EBW986, 23GBP589;   z) REF DYNDJ1057A, UDI/DI 40888277204790 (case), 10888277204799 (unit), Lot Numbers:  23DBC974",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 9,
          "item": {
            "Field": "Distribution pattern",
            "Value": "Distribution US nationwide including Puerto Rico, Canada, UAE, and Panama",
            "Status": "recorded"
          }
        }
      ]
    }
  ]
}