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  "name": "Medline procedure kits labeled as:   1) BILLINGS CLINIC SC HEAD & NECK, Pack Number DYNJ33656C;   2) BLEPH/RHINO PACK, Pack Number DYNJ64669A;   3) DB ENT CSTM PACK-LF, Pack Number DYNJ33585C;   4) DENTAL PACK, Pack Number DYNJ54064;   5) EAR PACK, Pack Number DYNJ68678C;   6) ENT HEAD NECK PACK, Pack Number DYNJ49023D;   7) ENT PACK, Pack Number DYNJ42564B;   8) ENT PACK, Pack Number DYNJ50572;   9) ENT PACK, Pack Number DYNJ45175B;   10) ENT PACK, Pack Number DYNJ65585A;   11) EP PACK, Pack Number DYNJ59171;   12) FUNCTIONAL ENDO SINUS WEILER, Pack Number DYNJ58857A;   13) HEAD & NECK, Pack Number DYNJ902987F;   14) HEAD & NECK PACK, Pack Number DYNJ61295B;   15) HEAD & NECK PACK, Pack Number DYNJ30234B;   16) HEAD & NECK PACK, Pack Number DYNJ50383;   17) HEAD & NECK PACK, Pack Number DYNJ36634K;   18) HEAD & NECK PACK, Pack Number DYNJ66399;   19) HEAD AND NECK PACK-LF, Pack Number DYNJ38402I;   20) MAJOR ENT HARPER PACK-LF, Pack Number DYNJ0161710I;   21) NASAL SINUS PACK-LF, Pack Number DYNJ0751486N;   22) NE NASAL, Pack Number DYNJ03130D;   23) ORL PACK, Pack Number DYNJ63705B;   24) SINUS PACK, Pack Number DYNJ50110B;   25) SINUS PACK, Pack Number DYNJ50110B;   26) T & A PACK, Pack Number DYNJ58811A;   27) THORACIC PACK, Pack Number DYNJ30731M;   28) THYROIDECTOMIE DIAGNOSTIQUE-LF, Pack Number DYNJ42678A;   29) TONSILS & ADENOIDS, Pack Number DYNJ69465;   30) TRANSPHENOIDAL PACK, Pack Number DYNJ46556B;",
  "description": "FDA recall Z-1461-2025 — MEDLINE INDUSTRIES, LP - Northfield is recalling Medline procedure kits labeled as:   1) BILLINGS CLINIC SC HEAD & NECK, Pack Number DYNJ33656C;   2) BLEPH/RHINO PACK, Pack Number DYNJ64669A;   3) DB ENT CSTM PACK-LF, Pack Number DYNJ33585C;   4) DENTAL PACK, Pack Number DYNJ54064;   5) EAR PACK, Pack Number DYNJ68678C;   6) ENT HEAD NECK PACK, Pack Number DYNJ49023D;   7) ENT PACK, Pack Number DYNJ42564B;   8) ENT PACK, Pack Number DYNJ50572;   9) ENT PACK, Pack Number DYNJ45175B;   10) ENT PACK, Pack Number DYNJ65585A;   11) EP PACK, Pack Number DYNJ59171;   12) FUNCTIONAL ENDO SINUS WEILER, Pack Number DYNJ58857A;   13) HEAD & NECK, Pack Number DYNJ902987F;   14) HEAD & NECK PACK, Pack Number DYNJ61295B;   15) HEAD & NECK PACK, Pack Number DYNJ30234B;   16) HEAD & NECK PACK, Pack Number DYNJ50383;   17) HEAD & NECK PACK, Pack Number DYNJ36634K;   18) HEAD & NECK PACK, Pack Number DYNJ66399;   19) HEAD AND NECK PACK-LF, Pack Number DYNJ38402I;   20) MAJOR ENT HARPER PACK-LF, Pack Number DYNJ0161710I;   21) NASAL SINUS PACK-LF, Pack Number DYNJ0751486N;   22) NE NASAL, Pack Number DYNJ03130D;   23) ORL PACK, Pack Number DYNJ63705B;   24) SINUS PACK, Pack Number DYNJ50110B;   25) SINUS PACK, Pack Number DYNJ50110B;   26) T & A PACK, Pack Number DYNJ58811A;   27) THORACIC PACK, Pack Number DYNJ30731M;   28) THYROIDECTOMIE DIAGNOSTIQUE-LF, Pack Number DYNJ42678A;   29) TONSILS & ADENOIDS, Pack Number DYNJ69465;   30) TRANSPHENOIDAL PACK, Pack Number DYNJ46556B; (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.",
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  "dateModified": "2026-06-24T07:02:03.626072+00:00",
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    "@type": "schema:MedicalDevice",
    "name": "Medline procedure kits labeled as:   1) BILLINGS CLINIC SC HEAD & NECK, Pack Number DYNJ33656C;   2) BLEPH/RHINO PACK, Pack Number DYNJ64669A;   3) DB ENT CSTM PACK-LF, Pack Number DYNJ33585C;   4) DENTAL PACK, Pack Number DYNJ54064;   5) EAR PACK, Pack Number DYNJ68678C;   6) ENT HEAD NECK PACK, Pack Number DYNJ49023D;   7) ENT PACK, Pack Number DYNJ42564B;   8) ENT PACK, Pack Number DYNJ50572;   9) ENT PACK, Pack Number DYNJ45175B;   10) ENT PACK, Pack Number DYNJ65585A;   11) EP PACK, Pack Number DYNJ59171;   12) FUNCTIONAL ENDO SINUS WEILER, Pack Number DYNJ58857A;   13) HEAD & NECK, Pack Number DYNJ902987F;   14) HEAD & NECK PACK, Pack Number DYNJ61295B;   15) HEAD & NECK PACK, Pack Number DYNJ30234B;   16) HEAD & NECK PACK, Pack Number DYNJ50383;   17) HEAD & NECK PACK, Pack Number DYNJ36634K;   18) HEAD & NECK PACK, Pack Number DYNJ66399;   19) HEAD AND NECK PACK-LF, Pack Number DYNJ38402I;   20) MAJOR ENT HARPER PACK-LF, Pack Number DYNJ0161710I;   21) NASAL SINUS PACK-LF, Pack Number DYNJ0751486N;   22) NE NASAL, Pack Number DYNJ03130D;   23) ORL PACK, Pack Number DYNJ63705B;   24) SINUS PACK, Pack Number DYNJ50110B;   25) SINUS PACK, Pack Number DYNJ50110B;   26) T & A PACK, Pack Number DYNJ58811A;   27) THORACIC PACK, Pack Number DYNJ30731M;   28) THYROIDECTOMIE DIAGNOSTIQUE-LF, Pack Number DYNJ42678A;   29) TONSILS & ADENOIDS, Pack Number DYNJ69465;   30) TRANSPHENOIDAL PACK, Pack Number DYNJ46556B;",
    "manufacturer": {
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      "name": "MEDLINE INDUSTRIES, LP - Northfield"
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    {
      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-1461-2025/enforcement-record",
      "@type": "schema:Claim",
      "name": "FDA recall Z-1461-2025: MEDLINE INDUSTRIES, LP - Northfield is recalling Medline procedure kits labeled as:   1) BILLINGS CLINIC SC HEAD & NECK, Pack Number DYNJ33656C;   2) BLEPH/RHINO PACK, Pack Number DYNJ64669A;   3) DB ENT CSTM PACK-LF, Pack Number DYNJ33585C;   4) DENTAL PACK, Pack Number DYNJ54064;   5) EAR PACK, Pack Number DYNJ68678C;   6) ENT HEAD NECK PACK, Pack Number DYNJ49023D;   7) ENT PACK, Pack Number DYNJ42564B;   8) ENT PACK, Pack Number DYNJ50572;   9) ENT PACK, Pack Number DYNJ45175B;   10) ENT PACK, Pack Number DYNJ65585A;   11) EP PACK, Pack Number DYNJ59171;   12) FUNCTIONAL ENDO SINUS WEILER, Pack Number DYNJ58857A;   13) HEAD & NECK, Pack Number DYNJ902987F;   14) HEAD & NECK PACK, Pack Number DYNJ61295B;   15) HEAD & NECK PACK, Pack Number DYNJ30234B;   16) HEAD & NECK PACK, Pack Number DYNJ50383;   17) HEAD & NECK PACK, Pack Number DYNJ36634K;   18) HEAD & NECK PACK, Pack Number DYNJ66399;   19) HEAD AND NECK PACK-LF, Pack Number DYNJ38402I;   20) MAJOR ENT HARPER PACK-LF, Pack Number DYNJ0161710I;   21) NASAL SINUS PACK-LF, Pack Number DYNJ0751486N;   22) NE NASAL, Pack Number DYNJ03130D;   23) ORL PACK, Pack Number DYNJ63705B;   24) SINUS PACK, Pack Number DYNJ50110B;   25) SINUS PACK, Pack Number DYNJ50110B;   26) T & A PACK, Pack Number DYNJ58811A;   27) THORACIC PACK, Pack Number DYNJ30731M;   28) THYROIDECTOMIE DIAGNOSTIQUE-LF, Pack Number DYNJ42678A;   29) TONSILS & ADENOIDS, Pack Number DYNJ69465;   30) TRANSPHENOIDAL PACK, Pack Number DYNJ46556B;",
      "text": "The FDA logged enforcement record Z-1461-2025: MEDLINE INDUSTRIES, LP - Northfield is voluntarily recalling Medline procedure kits labeled as:   1) BILLINGS CLINIC SC HEAD & NECK, Pack Number DYNJ33656C;   2) BLEPH/RHINO PACK, Pack Number DYNJ64669A;   3) DB ENT CSTM PACK-LF, Pack Number DYNJ33585C;   4) DENTAL PACK, Pack Number DYNJ54064;   5) EAR PACK, Pack Number DYNJ68678C;   6) ENT HEAD NECK PACK, Pack Number DYNJ49023D;   7) ENT PACK, Pack Number DYNJ42564B;   8) ENT PACK, Pack Number DYNJ50572;   9) ENT PACK, Pack Number DYNJ45175B;   10) ENT PACK, Pack Number DYNJ65585A;   11) EP PACK, Pack Number DYNJ59171;   12) FUNCTIONAL ENDO SINUS WEILER, Pack Number DYNJ58857A;   13) HEAD & NECK, Pack Number DYNJ902987F;   14) HEAD & NECK PACK, Pack Number DYNJ61295B;   15) HEAD & NECK PACK, Pack Number DYNJ30234B;   16) HEAD & NECK PACK, Pack Number DYNJ50383;   17) HEAD & NECK PACK, Pack Number DYNJ36634K;   18) HEAD & NECK PACK, Pack Number DYNJ66399;   19) HEAD AND NECK PACK-LF, Pack Number DYNJ38402I;   20) MAJOR ENT HARPER PACK-LF, Pack Number DYNJ0161710I;   21) NASAL SINUS PACK-LF, Pack Number DYNJ0751486N;   22) NE NASAL, Pack Number DYNJ03130D;   23) ORL PACK, Pack Number DYNJ63705B;   24) SINUS PACK, Pack Number DYNJ50110B;   25) SINUS PACK, Pack Number DYNJ50110B;   26) T & A PACK, Pack Number DYNJ58811A;   27) THORACIC PACK, Pack Number DYNJ30731M;   28) THYROIDECTOMIE DIAGNOSTIQUE-LF, Pack Number DYNJ42678A;   29) TONSILS & ADENOIDS, Pack Number DYNJ69465;   30) TRANSPHENOIDAL PACK, Pack Number DYNJ46556B; — reason: Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.. Status: Ongoing — the recall is still being carried out.. Initiated 2025-02-11. Affected lots/codes: 1) Pack Number DYNJ55316G:  UDI/DI 10889942278022 (each) 40889942278023 (case), Lot Number 20BDA583A;  2) Pack Number DYNJ37741B:  UDI/DI 10193489682212 (each) 40193489682213 (case), Lot Number 20BDB113A;  3) Pack Number DYNJ0809731F:  UDI/DI 10193489369892 (each) 40193489369893 (case), Lot Number 20FBS559A;  4) Pack Number DYNJ66665:  UDI/DI 10888277546394 (each) 40888277546395 (case), Lot Number 20FMA565A;  5) Pack Number DYNJ37707D:  UDI/DI 10193489258936 (each) 40193489258937 (case), Lot Number 20HKB321A;  6) Pack Number DYNJ64526A:  UDI/DI 10193489531589 (each) 40193489531580 (case), Lot Number 20HMC644A;  7) Pack Number DYNJ62755B:  UDI/DI 10193489296792 (each) 40193489296793 (case), Lot Number 20HMD066A;  8) Pack Number DYNJ61634B:  UDI/DI 10888277756168 (each) 40888277756169 (case), Lot Number 20HMD167A;  9) Pack Number DYNJ83129:  UDI/DI 10193489366815 (each) 40193489366816 (case), Lot Number 20JKA848A;  10) Pack Number DYNJ35906F:  UDI/DI 10193489718577 (each) 40193489718578 (case), Lot Number 20LBI228Z;  11) Pack Number DYNJ35906F:  UDI/DI 10193489397598 (each) 40193489397599 (case), Lot Number 20LBS935Z;  12) Pack Number DYNJCEN04C:  UDI/DI 10193489805413 (each) 40193489805414 (case), Lot Number 21BBI544A;  13) Pack Number DYNJ54684B:  UDI/DI 10193489551068 (each) 40193489551069 (case), Lot Number 21IMD870A;  14) Pack Number DYNJ44692D:  UDI/DI 10193489909869 (each) 40193489909860 (case), Lot Number 21IME024A;  15) Pack Number DYNJ0190688Q:  UDI/DI 10193489322644 (each) 40193489322645 (case), Lot Number 21IME395A;  16) Pack Number DYNJ64670B:  UDI/DI 10889942575701 (each) 40889942575702 (case), Lot Number 21IME484A;  17) Pack Number DYNJ30196F:  UDI/DI 10193489976625 (each) 40193489976626 (case), Lot Number 21IME728A;  18) Pack Number DYNJ51796G:  UDI/DI 10889942651887 (each) 40889942651888 (case), Lot Number 21IME769A;  19) Pack Number DYNJ39734D:  UDI/DI 10193489303940 (each) 40193489303941 (case), Lot Number 21IMH101A;  20) Pack Number DYNJ64208:  UDI/DI 10193489917703 (each) 40193489917704 (case), Lot Number 22FBW094A;  21) Pack Number DYNJ43522C:  UDI/DI 10195327176310 (each) 40195327176311 (case), Lot Number 22GBL783M;  22) Pack Number DYNJ59765A:  UDI/DI 10195327155780 (each) 40195327155781 (case), Lot Number 22GBM456Z;  23) Pack Number DYNJ54965:  UDI/DI 10889942275069 (each) 40889942275060 (case), Lot Number 22GMA060Z;  24) Pack Number DYNJ09866U:  UDI/DI 10195327230081 (each) 40195327230082 (case), Lot Number 22JBY434A;  25) Pack Number DYNJ45861B:  UDI/DI 10193489276510 (each) 40193489276511 (case), Lot Number 22KBC920Z;  26) Pack Number DYNJ27165V:  UDI/DI 10888277208872 (each) 40888277208873 (case), Lot Number 23CBN716A;  27) Pack Number DYNJ35449G:  UDI/DI 10195327040239 (each) 40195327040230 (case), Lot Number 23CBO497A;  28) Pack Number DYNJ62673A:  UDI/DI 10195327026592 (each) 40195327026593 (case), Lot Number 23CDC561A;  29) Pack Number DYNJ37636L:  UDI/DI 10195327299064 (each) 40195327299065 (case), Lot Number 23CLA003A;  30) Pack Number DYNJ24637J:  UDI/DI 10195327383596 (each) 40195327383597 (case), Lot Number 23GMC950A. A RECORDED FDA enforcement action (occurred=true).",
      "claimType": "official_fact",
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        "sourceUrl": "https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=Z-1461-2025&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-1461-2025&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-1461-2025/fda-classification",
      "@type": "schema:Claim",
      "name": "FDA classified recall Z-1461-2025 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": {
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        "adjudged": true,
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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-1461-2025&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-1461-2025&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-1461-2025/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."
    }
  ],
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      "name": "FDA recall details — Z-1461-2025",
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          "position": 1,
          "item": {
            "Field": "Recall number",
            "Value": "Z-1461-2025",
            "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": "Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 7,
          "item": {
            "Field": "Initiated",
            "Value": "2025-02-11",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 8,
          "item": {
            "Field": "Lot/code info",
            "Value": "1) Pack Number DYNJ55316G:  UDI/DI 10889942278022 (each) 40889942278023 (case), Lot Number 20BDA583A;  2) Pack Number DYNJ37741B:  UDI/DI 10193489682212 (each) 40193489682213 (case), Lot Number 20BDB113A;  3) Pack Number DYNJ0809731F:  UDI/DI 10193489369892 (each) 40193489369893 (case), Lot Number 20FBS559A;  4) Pack Number DYNJ66665:  UDI/DI 10888277546394 (each) 40888277546395 (case), Lot Number 20FMA565A;  5) Pack Number DYNJ37707D:  UDI/DI 10193489258936 (each) 40193489258937 (case), Lot Number 20HKB321A;  6) Pack Number DYNJ64526A:  UDI/DI 10193489531589 (each) 40193489531580 (case), Lot Number 20HMC644A;  7) Pack Number DYNJ62755B:  UDI/DI 10193489296792 (each) 40193489296793 (case), Lot Number 20HMD066A;  8) Pack Number DYNJ61634B:  UDI/DI 10888277756168 (each) 40888277756169 (case), Lot Number 20HMD167A;  9) Pack Number DYNJ83129:  UDI/DI 10193489366815 (each) 40193489366816 (case), Lot Number 20JKA848A;  10) Pack Number DYNJ35906F:  UDI/DI 10193489718577 (each) 40193489718578 (case), Lot Number 20LBI228Z;  11) Pack Number DYNJ35906F:  UDI/DI 10193489397598 (each) 40193489397599 (case), Lot Number 20LBS935Z;  12) Pack Number DYNJCEN04C:  UDI/DI 10193489805413 (each) 40193489805414 (case), Lot Number 21BBI544A;  13) Pack Number DYNJ54684B:  UDI/DI 10193489551068 (each) 40193489551069 (case), Lot Number 21IMD870A;  14) Pack Number DYNJ44692D:  UDI/DI 10193489909869 (each) 40193489909860 (case), Lot Number 21IME024A;  15) Pack Number DYNJ0190688Q:  UDI/DI 10193489322644 (each) 40193489322645 (case), Lot Number 21IME395A;  16) Pack Number DYNJ64670B:  UDI/DI 10889942575701 (each) 40889942575702 (case), Lot Number 21IME484A;  17) Pack Number DYNJ30196F:  UDI/DI 10193489976625 (each) 40193489976626 (case), Lot Number 21IME728A;  18) Pack Number DYNJ51796G:  UDI/DI 10889942651887 (each) 40889942651888 (case), Lot Number 21IME769A;  19) Pack Number DYNJ39734D:  UDI/DI 10193489303940 (each) 40193489303941 (case), Lot Number 21IMH101A;  20) Pack Number DYNJ64208:  UDI/DI 10193489917703 (each) 40193489917704 (case), Lot Number 22FBW094A;  21) Pack Number DYNJ43522C:  UDI/DI 10195327176310 (each) 40195327176311 (case), Lot Number 22GBL783M;  22) Pack Number DYNJ59765A:  UDI/DI 10195327155780 (each) 40195327155781 (case), Lot Number 22GBM456Z;  23) Pack Number DYNJ54965:  UDI/DI 10889942275069 (each) 40889942275060 (case), Lot Number 22GMA060Z;  24) Pack Number DYNJ09866U:  UDI/DI 10195327230081 (each) 40195327230082 (case), Lot Number 22JBY434A;  25) Pack Number DYNJ45861B:  UDI/DI 10193489276510 (each) 40193489276511 (case), Lot Number 22KBC920Z;  26) Pack Number DYNJ27165V:  UDI/DI 10888277208872 (each) 40888277208873 (case), Lot Number 23CBN716A;  27) Pack Number DYNJ35449G:  UDI/DI 10195327040239 (each) 40195327040230 (case), Lot Number 23CBO497A;  28) Pack Number DYNJ62673A:  UDI/DI 10195327026592 (each) 40195327026593 (case), Lot Number 23CDC561A;  29) Pack Number DYNJ37636L:  UDI/DI 10195327299064 (each) 40195327299065 (case), Lot Number 23CLA003A;  30) Pack Number DYNJ24637J:  UDI/DI 10195327383596 (each) 40195327383597 (case), Lot Number 23GMC950A",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 9,
          "item": {
            "Field": "Distribution pattern",
            "Value": "Worldwide distribution - US Nationwide and the country of Canada.",
            "Status": "recorded"
          }
        }
      ]
    }
  ]
}