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  "name": "Medline brand, medical procedure convenience kits, labeled as: 1) NEURO CRANIOTOMY CDS #36-RF, SKU CDS780119T;   2) NEURO KIT, SKU CDS981327Q;   3) NEURO POSTERIOR SPINE PACK-LF, SKU DYNJ0311501I;   4) ACOUSTIC NEUROMA PACK-LF, SKU DYNJ37741D;   5) SCRIPPS SW NEURO PACK-LF, SKU DYNJ39836C;   6) SCRIPPS SW NEURO PACK-LF, SKU DYNJ39836D;   7) NEURO BUNDLE-LF, SKU DYNJ40095A;   8) NEURO BUNDLE-LF, SKU DYNJ40095B;   9) NEURO BUNDLE-LF, SKU DYNJ40095C;   10) NEURO BUNDLE-LF, SKU DYNJ40095D;   11) NEURO PACK-LF, SKU DYNJ42844D;   12) WMC VP SHUNT PACK-LF, SKU DYNJ50629J;   13) NEURO PACK, SKU DYNJ54255A;   14) NEURO CHRISTUS, SKU DYNJ61190A;   15) NEURO KIT, SKU DYNJ62854B;   16) NEURO KIT, SKU DYNJ62854C;   17) NEURO PACK NTX, SKU DYNJ66213D;   18) NEURO PACK, SKU DYNJ67628C;   19) BASIC NEURO CUSTOM, SKU DYNJ83387;   20) BASIC NEURO CUSTOM, SKU DYNJ83387A;   21) HALY NEURO PACK, SKU DYNJ87308;   22) FHWC NEURO, SKU DYNJ906131B;   23) CRANI, SKU DYNJ907865;   24) KIT NEURO LAFAYETTE, SKU DYNJ908615C;   25) GENERAL NEURO, SKU DYNJ909744",
  "description": "FDA recall Z-0724-2025 — MEDLINE INDUSTRIES, LP - Northfield is recalling Medline brand, medical procedure convenience kits, labeled as: 1) NEURO CRANIOTOMY CDS #36-RF, SKU CDS780119T;   2) NEURO KIT, SKU CDS981327Q;   3) NEURO POSTERIOR SPINE PACK-LF, SKU DYNJ0311501I;   4) ACOUSTIC NEUROMA PACK-LF, SKU DYNJ37741D;   5) SCRIPPS SW NEURO PACK-LF, SKU DYNJ39836C;   6) SCRIPPS SW NEURO PACK-LF, SKU DYNJ39836D;   7) NEURO BUNDLE-LF, SKU DYNJ40095A;   8) NEURO BUNDLE-LF, SKU DYNJ40095B;   9) NEURO BUNDLE-LF, SKU DYNJ40095C;   10) NEURO BUNDLE-LF, SKU DYNJ40095D;   11) NEURO PACK-LF, SKU DYNJ42844D;   12) WMC VP SHUNT PACK-LF, SKU DYNJ50629J;   13) NEURO PACK, SKU DYNJ54255A;   14) NEURO CHRISTUS, SKU DYNJ61190A;   15) NEURO KIT, SKU DYNJ62854B;   16) NEURO KIT, SKU DYNJ62854C;   17) NEURO PACK NTX, SKU DYNJ66213D;   18) NEURO PACK, SKU DYNJ67628C;   19) BASIC NEURO CUSTOM, SKU DYNJ83387;   20) BASIC NEURO CUSTOM, SKU DYNJ83387A;   21) HALY NEURO PACK, SKU DYNJ87308;   22) FHWC NEURO, SKU DYNJ906131B;   23) CRANI, SKU DYNJ907865;   24) KIT NEURO LAFAYETTE, SKU DYNJ908615C;   25) GENERAL NEURO, SKU DYNJ909744 (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/",
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  "dateModified": "2026-06-24T07:02:03.626072+00:00",
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    "name": "openFDA drug & device enforcement (recall) reports",
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    "@type": "schema:MedicalDevice",
    "name": "Medline brand, medical procedure convenience kits, labeled as: 1) NEURO CRANIOTOMY CDS #36-RF, SKU CDS780119T;   2) NEURO KIT, SKU CDS981327Q;   3) NEURO POSTERIOR SPINE PACK-LF, SKU DYNJ0311501I;   4) ACOUSTIC NEUROMA PACK-LF, SKU DYNJ37741D;   5) SCRIPPS SW NEURO PACK-LF, SKU DYNJ39836C;   6) SCRIPPS SW NEURO PACK-LF, SKU DYNJ39836D;   7) NEURO BUNDLE-LF, SKU DYNJ40095A;   8) NEURO BUNDLE-LF, SKU DYNJ40095B;   9) NEURO BUNDLE-LF, SKU DYNJ40095C;   10) NEURO BUNDLE-LF, SKU DYNJ40095D;   11) NEURO PACK-LF, SKU DYNJ42844D;   12) WMC VP SHUNT PACK-LF, SKU DYNJ50629J;   13) NEURO PACK, SKU DYNJ54255A;   14) NEURO CHRISTUS, SKU DYNJ61190A;   15) NEURO KIT, SKU DYNJ62854B;   16) NEURO KIT, SKU DYNJ62854C;   17) NEURO PACK NTX, SKU DYNJ66213D;   18) NEURO PACK, SKU DYNJ67628C;   19) BASIC NEURO CUSTOM, SKU DYNJ83387;   20) BASIC NEURO CUSTOM, SKU DYNJ83387A;   21) HALY NEURO PACK, SKU DYNJ87308;   22) FHWC NEURO, SKU DYNJ906131B;   23) CRANI, SKU DYNJ907865;   24) KIT NEURO LAFAYETTE, SKU DYNJ908615C;   25) GENERAL NEURO, SKU DYNJ909744",
    "manufacturer": {
      "@type": "schema:Organization",
      "name": "MEDLINE INDUSTRIES, LP - Northfield"
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    {
      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-0724-2025/enforcement-record",
      "@type": "schema:Claim",
      "name": "FDA recall Z-0724-2025: MEDLINE INDUSTRIES, LP - Northfield is recalling Medline brand, medical procedure convenience kits, labeled as: 1) NEURO CRANIOTOMY CDS #36-RF, SKU CDS780119T;   2) NEURO KIT, SKU CDS981327Q;   3) NEURO POSTERIOR SPINE PACK-LF, SKU DYNJ0311501I;   4) ACOUSTIC NEUROMA PACK-LF, SKU DYNJ37741D;   5) SCRIPPS SW NEURO PACK-LF, SKU DYNJ39836C;   6) SCRIPPS SW NEURO PACK-LF, SKU DYNJ39836D;   7) NEURO BUNDLE-LF, SKU DYNJ40095A;   8) NEURO BUNDLE-LF, SKU DYNJ40095B;   9) NEURO BUNDLE-LF, SKU DYNJ40095C;   10) NEURO BUNDLE-LF, SKU DYNJ40095D;   11) NEURO PACK-LF, SKU DYNJ42844D;   12) WMC VP SHUNT PACK-LF, SKU DYNJ50629J;   13) NEURO PACK, SKU DYNJ54255A;   14) NEURO CHRISTUS, SKU DYNJ61190A;   15) NEURO KIT, SKU DYNJ62854B;   16) NEURO KIT, SKU DYNJ62854C;   17) NEURO PACK NTX, SKU DYNJ66213D;   18) NEURO PACK, SKU DYNJ67628C;   19) BASIC NEURO CUSTOM, SKU DYNJ83387;   20) BASIC NEURO CUSTOM, SKU DYNJ83387A;   21) HALY NEURO PACK, SKU DYNJ87308;   22) FHWC NEURO, SKU DYNJ906131B;   23) CRANI, SKU DYNJ907865;   24) KIT NEURO LAFAYETTE, SKU DYNJ908615C;   25) GENERAL NEURO, SKU DYNJ909744",
      "text": "The FDA logged enforcement record Z-0724-2025: MEDLINE INDUSTRIES, LP - Northfield is voluntarily recalling Medline brand, medical procedure convenience kits, labeled as: 1) NEURO CRANIOTOMY CDS #36-RF, SKU CDS780119T;   2) NEURO KIT, SKU CDS981327Q;   3) NEURO POSTERIOR SPINE PACK-LF, SKU DYNJ0311501I;   4) ACOUSTIC NEUROMA PACK-LF, SKU DYNJ37741D;   5) SCRIPPS SW NEURO PACK-LF, SKU DYNJ39836C;   6) SCRIPPS SW NEURO PACK-LF, SKU DYNJ39836D;   7) NEURO BUNDLE-LF, SKU DYNJ40095A;   8) NEURO BUNDLE-LF, SKU DYNJ40095B;   9) NEURO BUNDLE-LF, SKU DYNJ40095C;   10) NEURO BUNDLE-LF, SKU DYNJ40095D;   11) NEURO PACK-LF, SKU DYNJ42844D;   12) WMC VP SHUNT PACK-LF, SKU DYNJ50629J;   13) NEURO PACK, SKU DYNJ54255A;   14) NEURO CHRISTUS, SKU DYNJ61190A;   15) NEURO KIT, SKU DYNJ62854B;   16) NEURO KIT, SKU DYNJ62854C;   17) NEURO PACK NTX, SKU DYNJ66213D;   18) NEURO PACK, SKU DYNJ67628C;   19) BASIC NEURO CUSTOM, SKU DYNJ83387;   20) BASIC NEURO CUSTOM, SKU DYNJ83387A;   21) HALY NEURO PACK, SKU DYNJ87308;   22) FHWC NEURO, SKU DYNJ906131B;   23) CRANI, SKU DYNJ907865;   24) KIT NEURO LAFAYETTE, SKU DYNJ908615C;   25) GENERAL NEURO, SKU DYNJ909744 — reason: Surgical Patties & Surgical Strips in specific lots of Custom Convenience Kits were found to contain higher-than-expected levels of endotoxin within the raw material used to produce sterile Codman Surgical Patties and Strips that may have resulted in out-of-specification levels of endotoxin in those finished goods. Status: Ongoing — the recall is still being carried out.. Initiated 2024-11-06. Affected lots/codes: UDI-DI:  CDS780119T, 10888277762688 (each), 40888277762689 (case), Lot Numbers: 20EBU829; UDI-DI:  CDS981327Q, 10195327080365 (each), 40195327080366 (case), Lot Numbers: 22FMH830 22FMF883; UDI-DI:  DYNJ0311501I, 10889942265886 (each), 40889942265887 (case), Lot Numbers: 22DMF117; UDI-DI:  DYNJ37741D, 10195327548940 (each), 40195327548941 (case), Lot Numbers: 24EMD032; UDI-DI:  DYNJ39836C, 10193489510324 (each), 40193489510325 (case), Lot Numbers: 20JMB588 20GMD367 20EMB420 20CMC383 20CMA256; UDI-DI:  DYNJ39836D, 10193489477177 (each), 40193489477178 (case), Lot Numbers: 22EMA431 22CMC948 22BMD597 22AMG597 21JMF846 21IMA074 21GMF465 21GMC844 21CME103 21CMD623 21BMC249; UDI-DI:  DYNJ40095A, 10193489370690 (each), 40193489370691 (case), Lot Numbers: 21KME983 21JMB244 21JMB245 21HMA330 21EME688 21DME512 21CMA323 20LMD710 20HMB030; UDI-DI:  DYNJ40095B, 10195327068325 (each), 40195327068326 (case), Lot Numbers: 22GMB406 22EMA845 22CME763; UDI-DI:  DYNJ40095C, 10195327211028 (each), 40195327211029 (case), Lot Numbers: 22JMH236; UDI-DI:  DYNJ40095D, 10195327281250 (each), 40195327281251 (case), Lot Numbers: 24HMC151 24GMA340 24DMK362 24CMH592 24BMF793 24AMF590 24AMD886 23LMB475 23KMD199 23IMF930 23HMG523 23HMB850 23GMI744 23GMH136 23FMD605 23EMC157 23CME914 23BMC902 22LME175; UDI-DI:  DYNJ42844D, 10193489880564 (each), 40193489880565 (case), Lot Numbers: 22HBZ336; UDI-DI:  DYNJ50629J, 10195327081324 (each), 40195327081325 (case), Lot Numbers: 22FBF021; UDI-DI:  DYNJ54255A, 10889942765256 (each), 40889942765257 (case), Lot Numbers: 20LBO578 20HBM398 20FBW118 20EBG032 20DBF296; UDI-DI:  DYNJ61190A, 10193489453355 (each), 40193489453356 (case), Lot Numbers: 23HBX568 23GBU378 23EBU255 23EBB228 23CBK006 23BBF587 22LBP590 22LBO797 22KBH699 22JBI769 22IBF404 22HMF895 22EMH841 22DMI740 22CMH488 22CME013 21JME676 21IMG224 21IMB620 21GMC966 21EMB917 21BMD698 21BMD492 21BMB573; UDI-DI:  DYNJ62854B, 10193489324402 (each), 40193489324403 (case), Lot Numbers: 20HBA904; UDI-DI:  DYNJ62854C, 10193489426984 (each), 40193489426985 (case), Lot Numbers: 24ABR077 23LBT405 23KBM929 23GBJ934 23FBA134 23DBP199 23BBI534 22LBQ392 22IBU624 22DBO531 22DBE837 21LBF713 21LBF714 21KBW798 21KBU432 21IBO584 21EBS026 21EBS045 21ABD769 21ABF202 20JBF504; UDI-DI:  DYNJ66213D, 10195327345129 (each), 40195327345120 (case), Lot Numbers: 23IBN119 23HBT681 23GBA060 23FBF235 23DBR382 23CBI721; UDI-DI:  DYNJ67628C, 10195327690342 (each), 40195327690343 (case), Lot Numbers: 24HMA885; UDI-DI:  DYNJ83387, 10195327262945 (each), 40195327262946 (case), Lot Numbers: 22LBP363; UDI-DI:  DYNJ83387A, 10195327365684 (each), 40195327365685 (case), Lot Numbers: 23IBS038 23GBF619 23EBP127 23DBI802; UDI-DI:  DYNJ87308, 10198459025631 (each), 40198459025632 (case), Lot Numbers: 24GMB920; UDI-DI:  DYNJ906131B, 10193489932386 (each), 40193489932387 (case), Lot Numbers: 22FBP752 22EBI045 22EBH247; UDI-DI:  DYNJ907865, 10193489908725 (each), 40193489908726 (case), Lot Numbers: 22CMB545 22BMA169 21HMB808; UDI-DI:  DYNJ908615C, 10198459082702 (each), 40198459082703 (case), Lot Numbers: 24HBS615; UDI-DI:  DYNJ909744, 10195327465636 (each), 40195327465637 (case), Lot Numbers: 24ALA727 23JLA320. A RECORDED FDA enforcement action (occurred=true).",
      "claimType": "official_fact",
      "reviewStatus": "current",
      "commercialInfluence": false,
      "epistemicStatus": {
        "occurred": true,
        "supported": true,
        "adjudged": true,
        "operative": true
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      "grounding": {
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        "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-0724-2025&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-0724-2025&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-0724-2025/fda-classification",
      "@type": "schema:Claim",
      "name": "FDA classified recall Z-0724-2025 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": {
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        "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-0724-2025&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-0724-2025&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-0724-2025/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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      "name": "FDA recall details — Z-0724-2025",
      "numberOfItems": 9,
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          "position": 1,
          "item": {
            "Field": "Recall number",
            "Value": "Z-0724-2025",
            "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 - Northfield",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 6,
          "item": {
            "Field": "Reason",
            "Value": "Surgical Patties & Surgical Strips in specific lots of Custom Convenience Kits were found to contain higher-than-expected levels of endotoxin within the raw material used to produce sterile Codman Surgical Patties and Strips that may have resulted in out-of-specification levels of endotoxin in those finished goods",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 7,
          "item": {
            "Field": "Initiated",
            "Value": "2024-11-06",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 8,
          "item": {
            "Field": "Lot/code info",
            "Value": "UDI-DI:  CDS780119T, 10888277762688 (each), 40888277762689 (case), Lot Numbers: 20EBU829; UDI-DI:  CDS981327Q, 10195327080365 (each), 40195327080366 (case), Lot Numbers: 22FMH830 22FMF883; UDI-DI:  DYNJ0311501I, 10889942265886 (each), 40889942265887 (case), Lot Numbers: 22DMF117; UDI-DI:  DYNJ37741D, 10195327548940 (each), 40195327548941 (case), Lot Numbers: 24EMD032; UDI-DI:  DYNJ39836C, 10193489510324 (each), 40193489510325 (case), Lot Numbers: 20JMB588 20GMD367 20EMB420 20CMC383 20CMA256; UDI-DI:  DYNJ39836D, 10193489477177 (each), 40193489477178 (case), Lot Numbers: 22EMA431 22CMC948 22BMD597 22AMG597 21JMF846 21IMA074 21GMF465 21GMC844 21CME103 21CMD623 21BMC249; UDI-DI:  DYNJ40095A, 10193489370690 (each), 40193489370691 (case), Lot Numbers: 21KME983 21JMB244 21JMB245 21HMA330 21EME688 21DME512 21CMA323 20LMD710 20HMB030; UDI-DI:  DYNJ40095B, 10195327068325 (each), 40195327068326 (case), Lot Numbers: 22GMB406 22EMA845 22CME763; UDI-DI:  DYNJ40095C, 10195327211028 (each), 40195327211029 (case), Lot Numbers: 22JMH236; UDI-DI:  DYNJ40095D, 10195327281250 (each), 40195327281251 (case), Lot Numbers: 24HMC151 24GMA340 24DMK362 24CMH592 24BMF793 24AMF590 24AMD886 23LMB475 23KMD199 23IMF930 23HMG523 23HMB850 23GMI744 23GMH136 23FMD605 23EMC157 23CME914 23BMC902 22LME175; UDI-DI:  DYNJ42844D, 10193489880564 (each), 40193489880565 (case), Lot Numbers: 22HBZ336; UDI-DI:  DYNJ50629J, 10195327081324 (each), 40195327081325 (case), Lot Numbers: 22FBF021; UDI-DI:  DYNJ54255A, 10889942765256 (each), 40889942765257 (case), Lot Numbers: 20LBO578 20HBM398 20FBW118 20EBG032 20DBF296; UDI-DI:  DYNJ61190A, 10193489453355 (each), 40193489453356 (case), Lot Numbers: 23HBX568 23GBU378 23EBU255 23EBB228 23CBK006 23BBF587 22LBP590 22LBO797 22KBH699 22JBI769 22IBF404 22HMF895 22EMH841 22DMI740 22CMH488 22CME013 21JME676 21IMG224 21IMB620 21GMC966 21EMB917 21BMD698 21BMD492 21BMB573; UDI-DI:  DYNJ62854B, 10193489324402 (each), 40193489324403 (case), Lot Numbers: 20HBA904; UDI-DI:  DYNJ62854C, 10193489426984 (each), 40193489426985 (case), Lot Numbers: 24ABR077 23LBT405 23KBM929 23GBJ934 23FBA134 23DBP199 23BBI534 22LBQ392 22IBU624 22DBO531 22DBE837 21LBF713 21LBF714 21KBW798 21KBU432 21IBO584 21EBS026 21EBS045 21ABD769 21ABF202 20JBF504; UDI-DI:  DYNJ66213D, 10195327345129 (each), 40195327345120 (case), Lot Numbers: 23IBN119 23HBT681 23GBA060 23FBF235 23DBR382 23CBI721; UDI-DI:  DYNJ67628C, 10195327690342 (each), 40195327690343 (case), Lot Numbers: 24HMA885; UDI-DI:  DYNJ83387, 10195327262945 (each), 40195327262946 (case), Lot Numbers: 22LBP363; UDI-DI:  DYNJ83387A, 10195327365684 (each), 40195327365685 (case), Lot Numbers: 23IBS038 23GBF619 23EBP127 23DBI802; UDI-DI:  DYNJ87308, 10198459025631 (each), 40198459025632 (case), Lot Numbers: 24GMB920; UDI-DI:  DYNJ906131B, 10193489932386 (each), 40193489932387 (case), Lot Numbers: 22FBP752 22EBI045 22EBH247; UDI-DI:  DYNJ907865, 10193489908725 (each), 40193489908726 (case), Lot Numbers: 22CMB545 22BMA169 21HMB808; UDI-DI:  DYNJ908615C, 10198459082702 (each), 40198459082703 (case), Lot Numbers: 24HBS615; UDI-DI:  DYNJ909744, 10195327465636 (each), 40195327465637 (case), Lot Numbers: 24ALA727 23JLA320",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 9,
          "item": {
            "Field": "Distribution pattern",
            "Value": "US Nationwide. Canada.",
            "Status": "recorded"
          }
        }
      ]
    }
  ]
}