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  "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-0179-2025.jsonld",
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  "name": "Medline brand medical procedure convenience kits, labeled as:    1) NEW LONDON TOTAL KNEE CDS, REF CDS982519W;   2) HAND/FOOT CDS, REF CDS984003A;   3) SPECIAL PROCEDURE PACK, REF DYNJ32639C;   4) PK-ORTHO-MINOR, REF DYNJ39547B;   5) ANT CERV ADD ON PACK, REF DYNJ41229C;   6) NAVIGATIONAL SPINE FUSION, REF DYNJ45153B;   7) FEET, ELBOW, AND ANKLE TEGH-LF, REF DYNJ46719B;   8) PLASTIC HAND PACK TEGH-LF, REF DYNJ46739B;   9) CVL INSERTION KIT-LF, REF DYNJ48587A;   10) CVL INSERTION KIT-LF, REF DYNJ48587A;   11) ENSEMBLE SURPLUS LCA-LF, REF DYNJ48892C;   12) EXTREMITY PACK, REF DYNJ49301B;   13) ACL ACCESSORY PACK, REF DYNJ50952F;   14) SPINAL INJECTION PACK, REF DYNJ51383F;   15) FTMC ARTHROS BASIC SETUP-LF, REF DYNJ54602A;   16) MINOR EXTREMITY PACK, REF DYNJ55324G;   17) MINOR EXTREMITY PACK, REF DYNJ55324G;   18) D-SPINE SUPPLEMENT PACK, REF DYNJ58115A;   19) EXTREMITY PACK, REF DYNJ62877;   20) AHT LG KNEE ROLL, REF DYNJ64823;   21) CUSTOM ORTHO PACK, REF DYNJ83675;   22) DR SUNDAR SCS KIT, REF DYNJ85288A;   23) CENTRAL SCS TRIAL PACK, REF DYNJ85503;   24) TOTAL KNEE CDS-LF, REF DYNJ909569;   25) EXTREMITY PACK, REF SYNJ10253B;   26) CARROLLTON HIP FX, REF SYNJ910003A;   27) ARTHROSCOPY, REF SYNJ910004C",
  "description": "FDA recall Z-0179-2025 — MEDLINE INDUSTRIES, LP - Northfield is recalling Medline brand medical procedure convenience kits, labeled as:    1) NEW LONDON TOTAL KNEE CDS, REF CDS982519W;   2) HAND/FOOT CDS, REF CDS984003A;   3) SPECIAL PROCEDURE PACK, REF DYNJ32639C;   4) PK-ORTHO-MINOR, REF DYNJ39547B;   5) ANT CERV ADD ON PACK, REF DYNJ41229C;   6) NAVIGATIONAL SPINE FUSION, REF DYNJ45153B;   7) FEET, ELBOW, AND ANKLE TEGH-LF, REF DYNJ46719B;   8) PLASTIC HAND PACK TEGH-LF, REF DYNJ46739B;   9) CVL INSERTION KIT-LF, REF DYNJ48587A;   10) CVL INSERTION KIT-LF, REF DYNJ48587A;   11) ENSEMBLE SURPLUS LCA-LF, REF DYNJ48892C;   12) EXTREMITY PACK, REF DYNJ49301B;   13) ACL ACCESSORY PACK, REF DYNJ50952F;   14) SPINAL INJECTION PACK, REF DYNJ51383F;   15) FTMC ARTHROS BASIC SETUP-LF, REF DYNJ54602A;   16) MINOR EXTREMITY PACK, REF DYNJ55324G;   17) MINOR EXTREMITY PACK, REF DYNJ55324G;   18) D-SPINE SUPPLEMENT PACK, REF DYNJ58115A;   19) EXTREMITY PACK, REF DYNJ62877;   20) AHT LG KNEE ROLL, REF DYNJ64823;   21) CUSTOM ORTHO PACK, REF DYNJ83675;   22) DR SUNDAR SCS KIT, REF DYNJ85288A;   23) CENTRAL SCS TRIAL PACK, REF DYNJ85503;   24) TOTAL KNEE CDS-LF, REF DYNJ909569;   25) EXTREMITY PACK, REF SYNJ10253B;   26) CARROLLTON HIP FX, REF SYNJ910003A;   27) ARTHROSCOPY, REF SYNJ910004C (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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      "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-0179-2025&lang=eng",
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    "@type": "schema:MedicalDevice",
    "name": "Medline brand medical procedure convenience kits, labeled as:    1) NEW LONDON TOTAL KNEE CDS, REF CDS982519W;   2) HAND/FOOT CDS, REF CDS984003A;   3) SPECIAL PROCEDURE PACK, REF DYNJ32639C;   4) PK-ORTHO-MINOR, REF DYNJ39547B;   5) ANT CERV ADD ON PACK, REF DYNJ41229C;   6) NAVIGATIONAL SPINE FUSION, REF DYNJ45153B;   7) FEET, ELBOW, AND ANKLE TEGH-LF, REF DYNJ46719B;   8) PLASTIC HAND PACK TEGH-LF, REF DYNJ46739B;   9) CVL INSERTION KIT-LF, REF DYNJ48587A;   10) CVL INSERTION KIT-LF, REF DYNJ48587A;   11) ENSEMBLE SURPLUS LCA-LF, REF DYNJ48892C;   12) EXTREMITY PACK, REF DYNJ49301B;   13) ACL ACCESSORY PACK, REF DYNJ50952F;   14) SPINAL INJECTION PACK, REF DYNJ51383F;   15) FTMC ARTHROS BASIC SETUP-LF, REF DYNJ54602A;   16) MINOR EXTREMITY PACK, REF DYNJ55324G;   17) MINOR EXTREMITY PACK, REF DYNJ55324G;   18) D-SPINE SUPPLEMENT PACK, REF DYNJ58115A;   19) EXTREMITY PACK, REF DYNJ62877;   20) AHT LG KNEE ROLL, REF DYNJ64823;   21) CUSTOM ORTHO PACK, REF DYNJ83675;   22) DR SUNDAR SCS KIT, REF DYNJ85288A;   23) CENTRAL SCS TRIAL PACK, REF DYNJ85503;   24) TOTAL KNEE CDS-LF, REF DYNJ909569;   25) EXTREMITY PACK, REF SYNJ10253B;   26) CARROLLTON HIP FX, REF SYNJ910003A;   27) ARTHROSCOPY, REF SYNJ910004C",
    "manufacturer": {
      "@type": "schema:Organization",
      "name": "MEDLINE INDUSTRIES, LP - Northfield"
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    {
      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-0179-2025/enforcement-record",
      "@type": "schema:Claim",
      "name": "FDA recall Z-0179-2025: MEDLINE INDUSTRIES, LP - Northfield is recalling Medline brand medical procedure convenience kits, labeled as:    1) NEW LONDON TOTAL KNEE CDS, REF CDS982519W;   2) HAND/FOOT CDS, REF CDS984003A;   3) SPECIAL PROCEDURE PACK, REF DYNJ32639C;   4) PK-ORTHO-MINOR, REF DYNJ39547B;   5) ANT CERV ADD ON PACK, REF DYNJ41229C;   6) NAVIGATIONAL SPINE FUSION, REF DYNJ45153B;   7) FEET, ELBOW, AND ANKLE TEGH-LF, REF DYNJ46719B;   8) PLASTIC HAND PACK TEGH-LF, REF DYNJ46739B;   9) CVL INSERTION KIT-LF, REF DYNJ48587A;   10) CVL INSERTION KIT-LF, REF DYNJ48587A;   11) ENSEMBLE SURPLUS LCA-LF, REF DYNJ48892C;   12) EXTREMITY PACK, REF DYNJ49301B;   13) ACL ACCESSORY PACK, REF DYNJ50952F;   14) SPINAL INJECTION PACK, REF DYNJ51383F;   15) FTMC ARTHROS BASIC SETUP-LF, REF DYNJ54602A;   16) MINOR EXTREMITY PACK, REF DYNJ55324G;   17) MINOR EXTREMITY PACK, REF DYNJ55324G;   18) D-SPINE SUPPLEMENT PACK, REF DYNJ58115A;   19) EXTREMITY PACK, REF DYNJ62877;   20) AHT LG KNEE ROLL, REF DYNJ64823;   21) CUSTOM ORTHO PACK, REF DYNJ83675;   22) DR SUNDAR SCS KIT, REF DYNJ85288A;   23) CENTRAL SCS TRIAL PACK, REF DYNJ85503;   24) TOTAL KNEE CDS-LF, REF DYNJ909569;   25) EXTREMITY PACK, REF SYNJ10253B;   26) CARROLLTON HIP FX, REF SYNJ910003A;   27) ARTHROSCOPY, REF SYNJ910004C",
      "text": "The FDA logged enforcement record Z-0179-2025: MEDLINE INDUSTRIES, LP - Northfield is voluntarily recalling Medline brand medical procedure convenience kits, labeled as:    1) NEW LONDON TOTAL KNEE CDS, REF CDS982519W;   2) HAND/FOOT CDS, REF CDS984003A;   3) SPECIAL PROCEDURE PACK, REF DYNJ32639C;   4) PK-ORTHO-MINOR, REF DYNJ39547B;   5) ANT CERV ADD ON PACK, REF DYNJ41229C;   6) NAVIGATIONAL SPINE FUSION, REF DYNJ45153B;   7) FEET, ELBOW, AND ANKLE TEGH-LF, REF DYNJ46719B;   8) PLASTIC HAND PACK TEGH-LF, REF DYNJ46739B;   9) CVL INSERTION KIT-LF, REF DYNJ48587A;   10) CVL INSERTION KIT-LF, REF DYNJ48587A;   11) ENSEMBLE SURPLUS LCA-LF, REF DYNJ48892C;   12) EXTREMITY PACK, REF DYNJ49301B;   13) ACL ACCESSORY PACK, REF DYNJ50952F;   14) SPINAL INJECTION PACK, REF DYNJ51383F;   15) FTMC ARTHROS BASIC SETUP-LF, REF DYNJ54602A;   16) MINOR EXTREMITY PACK, REF DYNJ55324G;   17) MINOR EXTREMITY PACK, REF DYNJ55324G;   18) D-SPINE SUPPLEMENT PACK, REF DYNJ58115A;   19) EXTREMITY PACK, REF DYNJ62877;   20) AHT LG KNEE ROLL, REF DYNJ64823;   21) CUSTOM ORTHO PACK, REF DYNJ83675;   22) DR SUNDAR SCS KIT, REF DYNJ85288A;   23) CENTRAL SCS TRIAL PACK, REF DYNJ85503;   24) TOTAL KNEE CDS-LF, REF DYNJ909569;   25) EXTREMITY PACK, REF SYNJ10253B;   26) CARROLLTON HIP FX, REF SYNJ910003A;   27) ARTHROSCOPY, REF SYNJ910004C — reason: It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.. Status: Ongoing — the recall is still being carried out.. Initiated 2024-09-04. Affected lots/codes: 1) REF CDS982519W, UDI/DI 40195327389971 (each), 10195327389970 (case), Lot Numbers:  24BBQ775;  2) REF CDS984003A, UDI/DI 40888277002891 (each), 10888277002890 (case), Lot Numbers:  24ABG354;  3) REF DYNJ32639C, UDI/DI 40889942919223 (each), 10889942919222 (case), Lot Numbers:  23KBE944;  4) REF DYNJ39547B, UDI/DI 40193489760485 (each), 10193489760484 (case), Lot Numbers:  23LBO506;  5) REF DYNJ41229C, UDI/DI 40195327609727 (each), 10195327609726 (case), Lot Numbers:  24ABK563;  6) REF DYNJ45153B, UDI/DI 40195327235414 (each), 10195327235413 (case), Lot Numbers:  24ABD667;  7) REF DYNJ46719B, UDI/DI 40889942279303 (each), 10889942279302 (case), Lot Numbers:  23LBP194;  8) REF DYNJ46739B, UDI/DI 40889942314318 (each), 10889942314317 (case), Lot Numbers:  24ABG221;  9) REF DYNJ48587A, UDI/DI 40889942313106 (each), 10889942313105 (case), Lot Numbers:  23LBO732;  10) REF DYNJ48587A, UDI/DI 40889942313106 (each), 10889942313105 (case), Lot Numbers:  23KBO606;  11) REF DYNJ48892C, UDI/DI 40889942791768 (each), 10889942791767 (case), Lot Numbers:  23KBB893;  12) REF DYNJ49301B, UDI/DI 40889942686613 (each), 10889942686612 (case), Lot Numbers:  24ABB592;  13) REF DYNJ50952F, UDI/DI 40193489361668 (each), 10193489361667 (case), Lot Numbers:  23LBV189;  14) REF DYNJ51383F, UDI/DI 40193489225588 (each), 10193489225587 (case), Lot Numbers:  23LBS071;  15) REF DYNJ54602A, UDI/DI 40195327456673 (each), 10195327456672 (case), Lot Numbers:  23LBO084;  16) REF DYNJ55324G, UDI/DI 40195327433964 (each), 10195327433963 (case), Lot Numbers:  23LBL961;  17) REF DYNJ55324G, UDI/DI 40195327433964 (each), 10195327433963 (case), Lot Numbers:  23KBE137;  18) REF DYNJ58115A, UDI/DI 40195327582037 (each), 10195327582036 (case), Lot Numbers:  23LBL852;  19) REF DYNJ62877, UDI/DI 40193489695824 (each), 10193489695823 (case), Lot Numbers:  23LBV377;  20) REF DYNJ64823, UDI/DI 40193489221054 (each), 10193489221053 (case), Lot Numbers:  23LBK801;  21) REF DYNJ83675, UDI/DI 40195327296408 (each), 10195327296407 (case), Lot Numbers:  24ABG702;  22) REF DYNJ85288A, UDI/DI 40195327543083 (each), 10195327543082 (case), Lot Numbers:  24ABG603;  23) REF DYNJ85503, UDI/DI 40195327509904 (each), 10195327509903 (case), Lot Numbers:  23LBS030;  24) REF DYNJ909569, UDI/DI 40195327399703 (each), 10195327399702 (case), Lot Numbers:  24BBF009;  25) REF SYNJ10253B, UDI/DI 40193489373593 (each), 10193489373592 (case), Lot Numbers:  24ABG182;  26) REF SYNJ910003A, UDI/DI 40889942848448 (each), 10889942848447 (case), Lot Numbers:  24ABW931;  27) REF SYNJ910004C, UDI/DI 40195327246748 (each), 10195327246747 (case), Lot Numbers:  24BBC876. A RECORDED FDA enforcement action (occurred=true).",
      "claimType": "official_fact",
      "reviewStatus": "current",
      "commercialInfluence": false,
      "epistemicStatus": {
        "occurred": true,
        "supported": true,
        "adjudged": true,
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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-0179-2025&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-0179-2025&lang=eng"
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      "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-0179-2025/fda-classification",
      "@type": "schema:Claim",
      "name": "FDA classified recall Z-0179-2025 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": {
        "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-0179-2025&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-0179-2025&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-0179-2025/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-0179-2025",
      "numberOfItems": 9,
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          "position": 1,
          "item": {
            "Field": "Recall number",
            "Value": "Z-0179-2025",
            "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": "It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 7,
          "item": {
            "Field": "Initiated",
            "Value": "2024-09-04",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 8,
          "item": {
            "Field": "Lot/code info",
            "Value": "1) REF CDS982519W, UDI/DI 40195327389971 (each), 10195327389970 (case), Lot Numbers:  24BBQ775;  2) REF CDS984003A, UDI/DI 40888277002891 (each), 10888277002890 (case), Lot Numbers:  24ABG354;  3) REF DYNJ32639C, UDI/DI 40889942919223 (each), 10889942919222 (case), Lot Numbers:  23KBE944;  4) REF DYNJ39547B, UDI/DI 40193489760485 (each), 10193489760484 (case), Lot Numbers:  23LBO506;  5) REF DYNJ41229C, UDI/DI 40195327609727 (each), 10195327609726 (case), Lot Numbers:  24ABK563;  6) REF DYNJ45153B, UDI/DI 40195327235414 (each), 10195327235413 (case), Lot Numbers:  24ABD667;  7) REF DYNJ46719B, UDI/DI 40889942279303 (each), 10889942279302 (case), Lot Numbers:  23LBP194;  8) REF DYNJ46739B, UDI/DI 40889942314318 (each), 10889942314317 (case), Lot Numbers:  24ABG221;  9) REF DYNJ48587A, UDI/DI 40889942313106 (each), 10889942313105 (case), Lot Numbers:  23LBO732;  10) REF DYNJ48587A, UDI/DI 40889942313106 (each), 10889942313105 (case), Lot Numbers:  23KBO606;  11) REF DYNJ48892C, UDI/DI 40889942791768 (each), 10889942791767 (case), Lot Numbers:  23KBB893;  12) REF DYNJ49301B, UDI/DI 40889942686613 (each), 10889942686612 (case), Lot Numbers:  24ABB592;  13) REF DYNJ50952F, UDI/DI 40193489361668 (each), 10193489361667 (case), Lot Numbers:  23LBV189;  14) REF DYNJ51383F, UDI/DI 40193489225588 (each), 10193489225587 (case), Lot Numbers:  23LBS071;  15) REF DYNJ54602A, UDI/DI 40195327456673 (each), 10195327456672 (case), Lot Numbers:  23LBO084;  16) REF DYNJ55324G, UDI/DI 40195327433964 (each), 10195327433963 (case), Lot Numbers:  23LBL961;  17) REF DYNJ55324G, UDI/DI 40195327433964 (each), 10195327433963 (case), Lot Numbers:  23KBE137;  18) REF DYNJ58115A, UDI/DI 40195327582037 (each), 10195327582036 (case), Lot Numbers:  23LBL852;  19) REF DYNJ62877, UDI/DI 40193489695824 (each), 10193489695823 (case), Lot Numbers:  23LBV377;  20) REF DYNJ64823, UDI/DI 40193489221054 (each), 10193489221053 (case), Lot Numbers:  23LBK801;  21) REF DYNJ83675, UDI/DI 40195327296408 (each), 10195327296407 (case), Lot Numbers:  24ABG702;  22) REF DYNJ85288A, UDI/DI 40195327543083 (each), 10195327543082 (case), Lot Numbers:  24ABG603;  23) REF DYNJ85503, UDI/DI 40195327509904 (each), 10195327509903 (case), Lot Numbers:  23LBS030;  24) REF DYNJ909569, UDI/DI 40195327399703 (each), 10195327399702 (case), Lot Numbers:  24BBF009;  25) REF SYNJ10253B, UDI/DI 40193489373593 (each), 10193489373592 (case), Lot Numbers:  24ABG182;  26) REF SYNJ910003A, UDI/DI 40889942848448 (each), 10889942848447 (case), Lot Numbers:  24ABW931;  27) REF SYNJ910004C, UDI/DI 40195327246748 (each), 10195327246747 (case), Lot Numbers:  24BBC876",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 9,
          "item": {
            "Field": "Distribution pattern",
            "Value": "Worldwide distribution - US Nationwide and the countries of Canada, Panama.",
            "Status": "recorded"
          }
        }
      ]
    }
  ]
}