{
  "@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-1101-2024.jsonld",
  "@type": "schema:Dataset",
  "name": "MEDLINE Kits, trays, and packs labeled as follows:    a)\tASC MINOR THYROID CDS, REF CDS983682F;   b)\tBRONCHOSCOPY KIT, REF DYKE1718A;   c)\tBRONCHOSCOPY KIT, REF DYKE1718B;   d)\tDOUBLE CENTRAL LINE CAP CHANGE, REF DYNDC2214G;   e)\tENT PACK, REF DYNJ55334C;   f)\tENT PACK, REF DYNJ45175B;   g)\tENT PACK, REF DYNJ59030A;   h)\tENT PACK, REF DYNJ83416;   i)\tENT/EPISTAXIS TRAY, REF MNS2895;   j)\tENT/EPISTAXIS TRAY, REF MNS2895H;   k)\tHEAD & NECK PACK, REF DYNJ60166C;   l)\tHEAD AND NECK CDS, REF CDS983910K;   m)\tHEAD AND NECK PACK, REF DYNJ68872C;   n)\tHEAD AND NECK PACK, REF DYNJ46216J;   o)\tNASAL, REF CDS984899G;   p)\tNASAL, REF CDS984899I;   q)\tPACK,BRONCHOSCOPY, REF DYNJ65475A;   r)\tSINGLE CENTRAL LINE CAP CHANGE, REF DYNDC2213F;   s)\tT & A, REF CDS984895I;   t)\tT AND A, REF DYNJ36719C;   u)\tT AND A, REF DYNJ906741B;   v)\tT AND A CDS, REF CDS983362C;   w)\tT&A PACK, REF DYNJ33112I;   x)\tTONSIL CDS-LF, REF CDS980272L;   y)\tTRACH CARE KIT, REF DYNDJN001A",
  "description": "FDA recall Z-1101-2024 — MEDLINE INDUSTRIES, LP - Northfield is recalling MEDLINE Kits, trays, and packs labeled as follows:    a)\tASC MINOR THYROID CDS, REF CDS983682F;   b)\tBRONCHOSCOPY KIT, REF DYKE1718A;   c)\tBRONCHOSCOPY KIT, REF DYKE1718B;   d)\tDOUBLE CENTRAL LINE CAP CHANGE, REF DYNDC2214G;   e)\tENT PACK, REF DYNJ55334C;   f)\tENT PACK, REF DYNJ45175B;   g)\tENT PACK, REF DYNJ59030A;   h)\tENT PACK, REF DYNJ83416;   i)\tENT/EPISTAXIS TRAY, REF MNS2895;   j)\tENT/EPISTAXIS TRAY, REF MNS2895H;   k)\tHEAD & NECK PACK, REF DYNJ60166C;   l)\tHEAD AND NECK CDS, REF CDS983910K;   m)\tHEAD AND NECK PACK, REF DYNJ68872C;   n)\tHEAD AND NECK PACK, REF DYNJ46216J;   o)\tNASAL, REF CDS984899G;   p)\tNASAL, REF CDS984899I;   q)\tPACK,BRONCHOSCOPY, REF DYNJ65475A;   r)\tSINGLE CENTRAL LINE CAP CHANGE, REF DYNDC2213F;   s)\tT & A, REF CDS984895I;   t)\tT AND A, REF DYNJ36719C;   u)\tT AND A, REF DYNJ906741B;   v)\tT AND A CDS, REF CDS983362C;   w)\tT&A PACK, REF DYNJ33112I;   x)\tTONSIL CDS-LF, REF CDS980272L;   y)\tTRACH CARE KIT, REF DYNDJN001A (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/",
  "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-1101-2024&lang=eng",
  "about": {
    "@type": "schema:MedicalDevice",
    "name": "MEDLINE Kits, trays, and packs labeled as follows:    a)\tASC MINOR THYROID CDS, REF CDS983682F;   b)\tBRONCHOSCOPY KIT, REF DYKE1718A;   c)\tBRONCHOSCOPY KIT, REF DYKE1718B;   d)\tDOUBLE CENTRAL LINE CAP CHANGE, REF DYNDC2214G;   e)\tENT PACK, REF DYNJ55334C;   f)\tENT PACK, REF DYNJ45175B;   g)\tENT PACK, REF DYNJ59030A;   h)\tENT PACK, REF DYNJ83416;   i)\tENT/EPISTAXIS TRAY, REF MNS2895;   j)\tENT/EPISTAXIS TRAY, REF MNS2895H;   k)\tHEAD & NECK PACK, REF DYNJ60166C;   l)\tHEAD AND NECK CDS, REF CDS983910K;   m)\tHEAD AND NECK PACK, REF DYNJ68872C;   n)\tHEAD AND NECK PACK, REF DYNJ46216J;   o)\tNASAL, REF CDS984899G;   p)\tNASAL, REF CDS984899I;   q)\tPACK,BRONCHOSCOPY, REF DYNJ65475A;   r)\tSINGLE CENTRAL LINE CAP CHANGE, REF DYNDC2213F;   s)\tT & A, REF CDS984895I;   t)\tT AND A, REF DYNJ36719C;   u)\tT AND A, REF DYNJ906741B;   v)\tT AND A CDS, REF CDS983362C;   w)\tT&A PACK, REF DYNJ33112I;   x)\tTONSIL CDS-LF, REF CDS980272L;   y)\tTRACH CARE KIT, REF DYNDJN001A",
    "manufacturer": {
      "@type": "schema:Organization",
      "name": "MEDLINE INDUSTRIES, LP - Northfield"
    }
  },
  "claims": [
    {
      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-1101-2024/enforcement-record",
      "@type": "schema:Claim",
      "name": "FDA recall Z-1101-2024: MEDLINE INDUSTRIES, LP - Northfield is recalling MEDLINE Kits, trays, and packs labeled as follows:    a)\tASC MINOR THYROID CDS, REF CDS983682F;   b)\tBRONCHOSCOPY KIT, REF DYKE1718A;   c)\tBRONCHOSCOPY KIT, REF DYKE1718B;   d)\tDOUBLE CENTRAL LINE CAP CHANGE, REF DYNDC2214G;   e)\tENT PACK, REF DYNJ55334C;   f)\tENT PACK, REF DYNJ45175B;   g)\tENT PACK, REF DYNJ59030A;   h)\tENT PACK, REF DYNJ83416;   i)\tENT/EPISTAXIS TRAY, REF MNS2895;   j)\tENT/EPISTAXIS TRAY, REF MNS2895H;   k)\tHEAD & NECK PACK, REF DYNJ60166C;   l)\tHEAD AND NECK CDS, REF CDS983910K;   m)\tHEAD AND NECK PACK, REF DYNJ68872C;   n)\tHEAD AND NECK PACK, REF DYNJ46216J;   o)\tNASAL, REF CDS984899G;   p)\tNASAL, REF CDS984899I;   q)\tPACK,BRONCHOSCOPY, REF DYNJ65475A;   r)\tSINGLE CENTRAL LINE CAP CHANGE, REF DYNDC2213F;   s)\tT & A, REF CDS984895I;   t)\tT AND A, REF DYNJ36719C;   u)\tT AND A, REF DYNJ906741B;   v)\tT AND A CDS, REF CDS983362C;   w)\tT&A PACK, REF DYNJ33112I;   x)\tTONSIL CDS-LF, REF CDS980272L;   y)\tTRACH CARE KIT, REF DYNDJN001A",
      "text": "The FDA logged enforcement record Z-1101-2024: MEDLINE INDUSTRIES, LP - Northfield is voluntarily recalling MEDLINE Kits, trays, and packs labeled as follows:    a)\tASC MINOR THYROID CDS, REF CDS983682F;   b)\tBRONCHOSCOPY KIT, REF DYKE1718A;   c)\tBRONCHOSCOPY KIT, REF DYKE1718B;   d)\tDOUBLE CENTRAL LINE CAP CHANGE, REF DYNDC2214G;   e)\tENT PACK, REF DYNJ55334C;   f)\tENT PACK, REF DYNJ45175B;   g)\tENT PACK, REF DYNJ59030A;   h)\tENT PACK, REF DYNJ83416;   i)\tENT/EPISTAXIS TRAY, REF MNS2895;   j)\tENT/EPISTAXIS TRAY, REF MNS2895H;   k)\tHEAD & NECK PACK, REF DYNJ60166C;   l)\tHEAD AND NECK CDS, REF CDS983910K;   m)\tHEAD AND NECK PACK, REF DYNJ68872C;   n)\tHEAD AND NECK PACK, REF DYNJ46216J;   o)\tNASAL, REF CDS984899G;   p)\tNASAL, REF CDS984899I;   q)\tPACK,BRONCHOSCOPY, REF DYNJ65475A;   r)\tSINGLE CENTRAL LINE CAP CHANGE, REF DYNDC2213F;   s)\tT & A, REF CDS984895I;   t)\tT AND A, REF DYNJ36719C;   u)\tT AND A, REF DYNJ906741B;   v)\tT AND A CDS, REF CDS983362C;   w)\tT&A PACK, REF DYNJ33112I;   x)\tTONSIL CDS-LF, REF CDS980272L;   y)\tTRACH CARE KIT, REF DYNDJN001A — 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 CDS983682F; UDI/DI 40193489852975 (case), 10193489852974 (unit), lot Numbers:  22DDA235, 22GBJ113, 23ABQ437, 23EBS939;   b) REF DYKE1718A; UDI/DI 40193489494656 (case), 10193489494655 (unit), Lot Numbers:  22FBU098, 22HBM601, 23ABM389;   c) REF DYKE1718B; UDI/DI 40195327240128 (case), 10195327240127 (unit), Lot Numbers:  23DBE977;   d) REF DYNDC2214G; UDI/DI 40195327051984 (case), 10195327051983 (unit), Lot Numbers:  22ABP471, 22BBO794, 22OBJ991;     e) REF DYNJ55334C; UDI/DI 40889942703211 (case), 10889942703210 (unit), Lot Numbers:  22ABL051, 22EBV190, 22FBS394, 23BBA777, 23GBL169;   f) REF DYNJ45175B; UDI/DI 40889942485216 (case), 10889942485215 (unit), Lot Numbers:  22CLB148, 22GLB002;   g) REF DYNJ59030A; UDI/DI 40195327026203 (cases), 10195327026202 (unit), Lot Numbers:  22DBR838, 22EBO071, 22JBW765, 23FBF261, 23GBC456, 23HBR618;   h) REF DYNJ83416; UDI/DI 40195327265053 (cases), 10195327265052 (unit), Lot Numbers:  22LBF471, 23ABN102, 23BBA471;   i) REF MNS2895; UDI/DI 50653160062934 (case), 653160062939 (unit), Lot Numbers:  23BBQ180, 23DBN766, 23EBH195, 23FBE540;   j) REF MNS2895H; UDI/DI 50653160062934 (case), 653160062939 (unit), Lot Numbers:  23BBQ180, 23DBN766, 23EBH195, 23FBE540;   k) REF DYNJ60166C; UDI/DI 40193489467148 (case), 10193489467147 (unit), Lot Numbers:  23ELB099;   l) REF CDS983910K; UDI/DI 40195327256594 (case), 10195327256593 (unit), Lot Numbers:  22JBT244, 23ABP271, 23ABP272, 23ABQ792, 23CBE912, 23DBR779, 23FBB371, 23JBL006, 23JBR337;   m) REF DYNJ68872C; UDI/DI 40195327375714 (case), 10195327375713 (unit), Lot Numbers:  23DBC646, 23FBA039, 23GBA604, 23HBZ389, 23JBN556;   n) REF DYNJ46216J; UDI/DI 40195327407491 (case), 10195327407490 (unit), Lot Numbers:  23EBF873, 23GBO919, 23GBT576, 23IBE145;   o) REF CDS984899G; UDI/DI 40193489983822 (case), 10193489983821 (unit), Lot Numbers:  22CLA789;   p) REF CDS984899I; UDI/DI 40195327313297 (case), 10195327313296 (unit), Lot Numbers:  23IBV180;   q) REF DYNJ65475A; UDI/DI 40193489974578 (case), 10193489974577 (unit), Lot Numbers:  22DBF905;   r) REF DYNDC2213F; UDI/DI 40195327052080 (case), 10195327052089 (unit), Lot number:  22ABM936, 22CMG684, 22EMB991;   s) REF CDS984895I; UDI/DI 40193489983815 (case), 10193489983814 (unit), Lot Number:  22FBL382, 22IBD790, 23ABM451, 23DBM334;   t) REF DYNJ36719C; UDI/DI 40193489265539 (case), 10193489265538 (unit), Lot Numbers:  21LBA818, 21LBU235, 22BBL912;   u) REF DYNJ906741B; UDI/DI 40195327055364 (case), 10195327055363 (unit), Lot Numbers:  22ABF704, 22ABL214, 22BBQ966, 22FBY564, 22GBQ902, 22HMI302, 23AMA387, 23AMI317;   v) REF CDS983362C; UDI/DI 40193489267342 (case), 10193489267341 (unit), Lot Numbers:  23ABI733;   w) REF DYNJ33112I; UDI/DI 40193489402736 (case), 10193489402735 (unit), Lot Numbers:  22DBO140, 22DBO155, 22JBY668, 23BBT134, 23DBT051, 23EBA549, 23HBI328, 23IBM005;   x) REF CDS980272L; UDI/DI 40193489616331 (case), 10193489616330 (unit), Lot Numbers:  22NBC732;   y) REF DYNDJN001A; UDI/DI 40193489421614 (case), 10193489421613 (unit), Lot Numbers:  22EBB217, 22FBQ070, 22FBU496. 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-1101-2024&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-1101-2024&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-1101-2024/fda-classification",
      "@type": "schema:Claim",
      "name": "FDA classified recall Z-1101-2024 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-1101-2024&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-1101-2024&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-1101-2024/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-1101-2024",
      "numberOfItems": 9,
      "itemListElement": [
        {
          "@type": "schema:ListItem",
          "position": 1,
          "item": {
            "Field": "Recall number",
            "Value": "Z-1101-2024",
            "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 CDS983682F; UDI/DI 40193489852975 (case), 10193489852974 (unit), lot Numbers:  22DDA235, 22GBJ113, 23ABQ437, 23EBS939;   b) REF DYKE1718A; UDI/DI 40193489494656 (case), 10193489494655 (unit), Lot Numbers:  22FBU098, 22HBM601, 23ABM389;   c) REF DYKE1718B; UDI/DI 40195327240128 (case), 10195327240127 (unit), Lot Numbers:  23DBE977;   d) REF DYNDC2214G; UDI/DI 40195327051984 (case), 10195327051983 (unit), Lot Numbers:  22ABP471, 22BBO794, 22OBJ991;     e) REF DYNJ55334C; UDI/DI 40889942703211 (case), 10889942703210 (unit), Lot Numbers:  22ABL051, 22EBV190, 22FBS394, 23BBA777, 23GBL169;   f) REF DYNJ45175B; UDI/DI 40889942485216 (case), 10889942485215 (unit), Lot Numbers:  22CLB148, 22GLB002;   g) REF DYNJ59030A; UDI/DI 40195327026203 (cases), 10195327026202 (unit), Lot Numbers:  22DBR838, 22EBO071, 22JBW765, 23FBF261, 23GBC456, 23HBR618;   h) REF DYNJ83416; UDI/DI 40195327265053 (cases), 10195327265052 (unit), Lot Numbers:  22LBF471, 23ABN102, 23BBA471;   i) REF MNS2895; UDI/DI 50653160062934 (case), 653160062939 (unit), Lot Numbers:  23BBQ180, 23DBN766, 23EBH195, 23FBE540;   j) REF MNS2895H; UDI/DI 50653160062934 (case), 653160062939 (unit), Lot Numbers:  23BBQ180, 23DBN766, 23EBH195, 23FBE540;   k) REF DYNJ60166C; UDI/DI 40193489467148 (case), 10193489467147 (unit), Lot Numbers:  23ELB099;   l) REF CDS983910K; UDI/DI 40195327256594 (case), 10195327256593 (unit), Lot Numbers:  22JBT244, 23ABP271, 23ABP272, 23ABQ792, 23CBE912, 23DBR779, 23FBB371, 23JBL006, 23JBR337;   m) REF DYNJ68872C; UDI/DI 40195327375714 (case), 10195327375713 (unit), Lot Numbers:  23DBC646, 23FBA039, 23GBA604, 23HBZ389, 23JBN556;   n) REF DYNJ46216J; UDI/DI 40195327407491 (case), 10195327407490 (unit), Lot Numbers:  23EBF873, 23GBO919, 23GBT576, 23IBE145;   o) REF CDS984899G; UDI/DI 40193489983822 (case), 10193489983821 (unit), Lot Numbers:  22CLA789;   p) REF CDS984899I; UDI/DI 40195327313297 (case), 10195327313296 (unit), Lot Numbers:  23IBV180;   q) REF DYNJ65475A; UDI/DI 40193489974578 (case), 10193489974577 (unit), Lot Numbers:  22DBF905;   r) REF DYNDC2213F; UDI/DI 40195327052080 (case), 10195327052089 (unit), Lot number:  22ABM936, 22CMG684, 22EMB991;   s) REF CDS984895I; UDI/DI 40193489983815 (case), 10193489983814 (unit), Lot Number:  22FBL382, 22IBD790, 23ABM451, 23DBM334;   t) REF DYNJ36719C; UDI/DI 40193489265539 (case), 10193489265538 (unit), Lot Numbers:  21LBA818, 21LBU235, 22BBL912;   u) REF DYNJ906741B; UDI/DI 40195327055364 (case), 10195327055363 (unit), Lot Numbers:  22ABF704, 22ABL214, 22BBQ966, 22FBY564, 22GBQ902, 22HMI302, 23AMA387, 23AMI317;   v) REF CDS983362C; UDI/DI 40193489267342 (case), 10193489267341 (unit), Lot Numbers:  23ABI733;   w) REF DYNJ33112I; UDI/DI 40193489402736 (case), 10193489402735 (unit), Lot Numbers:  22DBO140, 22DBO155, 22JBY668, 23BBT134, 23DBT051, 23EBA549, 23HBI328, 23IBM005;   x) REF CDS980272L; UDI/DI 40193489616331 (case), 10193489616330 (unit), Lot Numbers:  22NBC732;   y) REF DYNDJN001A; UDI/DI 40193489421614 (case), 10193489421613 (unit), Lot Numbers:  22EBB217, 22FBQ070, 22FBU496",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 9,
          "item": {
            "Field": "Distribution pattern",
            "Value": "Distribution US nationwide including Puerto Rico, Canada, UAE, and Panama",
            "Status": "recorded"
          }
        }
      ]
    }
  ]
}