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  "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-0160-2025.jsonld",
  "@type": "schema:Dataset",
  "name": "Medline brand medical procedure convenience kits, labeled as:    1) T&A CDS-LF, REF CDS982091I;   2) TONSIL CDS, REF CDS984492B;   3) RV T&A PACK-LF, REF DYNJ0798129I;   4) DIRECT MICRO LARYNG PK-LF, REF DYNJ30591I;   5) APU LINE PACK, REF DYNJ37171A;   6) T&A PACK-LF, REF DYNJ40836F;   7) ENT PACK, REF DYNJ44249J;   8) TONSIL PACK, REF DYNJ44349L;   9) TONSIL PACK, REF DYNJ44349M;   10) NASAL PACK, REF DYNJ53200C;   11) TONSIL & ADENOIDS PACK, REF DYNJ53270C;   12) FTMC MYRINGOTOMY PACK-LF, REF DYNJ54610A;   13) HEAD AND NECK PACK, REF DYNJ55255C;   14) ENT T&A PACK, REF DYNJ58979;   15) EENT PACK, REF DYNJ62927;   16) ENT, REF DYNJ63190A;   17) D L B PACK, REF DYNJ66274A;   18) ASC T&A, REF DYNJ67109B;   19) TONSIL T AND A PACK SHD, REF DYNJ68417C;   20) T A PACK, REF DYNJ80227B;   21) TONSIL AND ADENOID PACK, REF DYNJ80559A;   22) T AND A PACK UMMC KIT, REF DYNJ81880;   23) T/A ENDO PACK, REF DYNJ83158;   24) JVL - MODULE T A  PK, REF DYNJ84083;   25) T&A, REF DYNJ900289J;   26) T&A, REF DYNJ900289J;   27) T & A, REF DYNJ902626G;   28) LARYNGOSCOPY BRONCH-LF, REF DYNJ903264A;   29) T&A, REF DYNJ903428J;   30) T&A, REF DYNJ903428J;   31) PEDI ENT - OAKBEND, REF DYNJ905769;   32) T & A, REF DYNJ907056C;   33) ASC FARRELL T&A, REF DYNJ908132;   34) CHS ENT PACK, REF DYNJCH500",
  "description": "FDA recall Z-0160-2025 — MEDLINE INDUSTRIES, LP - Northfield is recalling Medline brand medical procedure convenience kits, labeled as:    1) T&A CDS-LF, REF CDS982091I;   2) TONSIL CDS, REF CDS984492B;   3) RV T&A PACK-LF, REF DYNJ0798129I;   4) DIRECT MICRO LARYNG PK-LF, REF DYNJ30591I;   5) APU LINE PACK, REF DYNJ37171A;   6) T&A PACK-LF, REF DYNJ40836F;   7) ENT PACK, REF DYNJ44249J;   8) TONSIL PACK, REF DYNJ44349L;   9) TONSIL PACK, REF DYNJ44349M;   10) NASAL PACK, REF DYNJ53200C;   11) TONSIL & ADENOIDS PACK, REF DYNJ53270C;   12) FTMC MYRINGOTOMY PACK-LF, REF DYNJ54610A;   13) HEAD AND NECK PACK, REF DYNJ55255C;   14) ENT T&A PACK, REF DYNJ58979;   15) EENT PACK, REF DYNJ62927;   16) ENT, REF DYNJ63190A;   17) D L B PACK, REF DYNJ66274A;   18) ASC T&A, REF DYNJ67109B;   19) TONSIL T AND A PACK SHD, REF DYNJ68417C;   20) T A PACK, REF DYNJ80227B;   21) TONSIL AND ADENOID PACK, REF DYNJ80559A;   22) T AND A PACK UMMC KIT, REF DYNJ81880;   23) T/A ENDO PACK, REF DYNJ83158;   24) JVL - MODULE T A  PK, REF DYNJ84083;   25) T&A, REF DYNJ900289J;   26) T&A, REF DYNJ900289J;   27) T & A, REF DYNJ902626G;   28) LARYNGOSCOPY BRONCH-LF, REF DYNJ903264A;   29) T&A, REF DYNJ903428J;   30) T&A, REF DYNJ903428J;   31) PEDI ENT - OAKBEND, REF DYNJ905769;   32) T & A, REF DYNJ907056C;   33) ASC FARRELL T&A, REF DYNJ908132;   34) CHS ENT PACK, REF DYNJCH500 (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 brand medical procedure convenience kits, labeled as:    1) T&A CDS-LF, REF CDS982091I;   2) TONSIL CDS, REF CDS984492B;   3) RV T&A PACK-LF, REF DYNJ0798129I;   4) DIRECT MICRO LARYNG PK-LF, REF DYNJ30591I;   5) APU LINE PACK, REF DYNJ37171A;   6) T&A PACK-LF, REF DYNJ40836F;   7) ENT PACK, REF DYNJ44249J;   8) TONSIL PACK, REF DYNJ44349L;   9) TONSIL PACK, REF DYNJ44349M;   10) NASAL PACK, REF DYNJ53200C;   11) TONSIL & ADENOIDS PACK, REF DYNJ53270C;   12) FTMC MYRINGOTOMY PACK-LF, REF DYNJ54610A;   13) HEAD AND NECK PACK, REF DYNJ55255C;   14) ENT T&A PACK, REF DYNJ58979;   15) EENT PACK, REF DYNJ62927;   16) ENT, REF DYNJ63190A;   17) D L B PACK, REF DYNJ66274A;   18) ASC T&A, REF DYNJ67109B;   19) TONSIL T AND A PACK SHD, REF DYNJ68417C;   20) T A PACK, REF DYNJ80227B;   21) TONSIL AND ADENOID PACK, REF DYNJ80559A;   22) T AND A PACK UMMC KIT, REF DYNJ81880;   23) T/A ENDO PACK, REF DYNJ83158;   24) JVL - MODULE T A  PK, REF DYNJ84083;   25) T&A, REF DYNJ900289J;   26) T&A, REF DYNJ900289J;   27) T & A, REF DYNJ902626G;   28) LARYNGOSCOPY BRONCH-LF, REF DYNJ903264A;   29) T&A, REF DYNJ903428J;   30) T&A, REF DYNJ903428J;   31) PEDI ENT - OAKBEND, REF DYNJ905769;   32) T & A, REF DYNJ907056C;   33) ASC FARRELL T&A, REF DYNJ908132;   34) CHS ENT PACK, REF DYNJCH500",
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      "name": "MEDLINE INDUSTRIES, LP - Northfield"
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    {
      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-0160-2025/enforcement-record",
      "@type": "schema:Claim",
      "name": "FDA recall Z-0160-2025: MEDLINE INDUSTRIES, LP - Northfield is recalling Medline brand medical procedure convenience kits, labeled as:    1) T&A CDS-LF, REF CDS982091I;   2) TONSIL CDS, REF CDS984492B;   3) RV T&A PACK-LF, REF DYNJ0798129I;   4) DIRECT MICRO LARYNG PK-LF, REF DYNJ30591I;   5) APU LINE PACK, REF DYNJ37171A;   6) T&A PACK-LF, REF DYNJ40836F;   7) ENT PACK, REF DYNJ44249J;   8) TONSIL PACK, REF DYNJ44349L;   9) TONSIL PACK, REF DYNJ44349M;   10) NASAL PACK, REF DYNJ53200C;   11) TONSIL & ADENOIDS PACK, REF DYNJ53270C;   12) FTMC MYRINGOTOMY PACK-LF, REF DYNJ54610A;   13) HEAD AND NECK PACK, REF DYNJ55255C;   14) ENT T&A PACK, REF DYNJ58979;   15) EENT PACK, REF DYNJ62927;   16) ENT, REF DYNJ63190A;   17) D L B PACK, REF DYNJ66274A;   18) ASC T&A, REF DYNJ67109B;   19) TONSIL T AND A PACK SHD, REF DYNJ68417C;   20) T A PACK, REF DYNJ80227B;   21) TONSIL AND ADENOID PACK, REF DYNJ80559A;   22) T AND A PACK UMMC KIT, REF DYNJ81880;   23) T/A ENDO PACK, REF DYNJ83158;   24) JVL - MODULE T A  PK, REF DYNJ84083;   25) T&A, REF DYNJ900289J;   26) T&A, REF DYNJ900289J;   27) T & A, REF DYNJ902626G;   28) LARYNGOSCOPY BRONCH-LF, REF DYNJ903264A;   29) T&A, REF DYNJ903428J;   30) T&A, REF DYNJ903428J;   31) PEDI ENT - OAKBEND, REF DYNJ905769;   32) T & A, REF DYNJ907056C;   33) ASC FARRELL T&A, REF DYNJ908132;   34) CHS ENT PACK, REF DYNJCH500",
      "text": "The FDA logged enforcement record Z-0160-2025: MEDLINE INDUSTRIES, LP - Northfield is voluntarily recalling Medline brand medical procedure convenience kits, labeled as:    1) T&A CDS-LF, REF CDS982091I;   2) TONSIL CDS, REF CDS984492B;   3) RV T&A PACK-LF, REF DYNJ0798129I;   4) DIRECT MICRO LARYNG PK-LF, REF DYNJ30591I;   5) APU LINE PACK, REF DYNJ37171A;   6) T&A PACK-LF, REF DYNJ40836F;   7) ENT PACK, REF DYNJ44249J;   8) TONSIL PACK, REF DYNJ44349L;   9) TONSIL PACK, REF DYNJ44349M;   10) NASAL PACK, REF DYNJ53200C;   11) TONSIL & ADENOIDS PACK, REF DYNJ53270C;   12) FTMC MYRINGOTOMY PACK-LF, REF DYNJ54610A;   13) HEAD AND NECK PACK, REF DYNJ55255C;   14) ENT T&A PACK, REF DYNJ58979;   15) EENT PACK, REF DYNJ62927;   16) ENT, REF DYNJ63190A;   17) D L B PACK, REF DYNJ66274A;   18) ASC T&A, REF DYNJ67109B;   19) TONSIL T AND A PACK SHD, REF DYNJ68417C;   20) T A PACK, REF DYNJ80227B;   21) TONSIL AND ADENOID PACK, REF DYNJ80559A;   22) T AND A PACK UMMC KIT, REF DYNJ81880;   23) T/A ENDO PACK, REF DYNJ83158;   24) JVL - MODULE T A  PK, REF DYNJ84083;   25) T&A, REF DYNJ900289J;   26) T&A, REF DYNJ900289J;   27) T & A, REF DYNJ902626G;   28) LARYNGOSCOPY BRONCH-LF, REF DYNJ903264A;   29) T&A, REF DYNJ903428J;   30) T&A, REF DYNJ903428J;   31) PEDI ENT - OAKBEND, REF DYNJ905769;   32) T & A, REF DYNJ907056C;   33) ASC FARRELL T&A, REF DYNJ908132;   34) CHS ENT PACK, REF DYNJCH500 — 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 CDS982091I, UDI/DI 40193489741644 (each), 10193489741643 (case), Lot Numbers:  24BBA623;  2) REF CDS984492B, UDI/DI 40193489637183 (each), 10193489637182 (case), Lot Numbers:  24ABB114;  3) REF DYNJ0798129I, UDI/DI 40195327226511 (each), 10195327226510 (case), Lot Numbers:  23KBB859;  4) REF DYNJ30591I, UDI/DI 40193489962841 (each), 10193489962840 (case), Lot Numbers:  24ABD228;  5) REF DYNJ37171A, UDI/DI 40884389750620 (each), 10884389750629 (case), Lot Numbers:  23KBD998;  6) REF DYNJ40836F, UDI/DI 40195327059539 (each), 10195327059538 (case), Lot Numbers:  23LBQ627;  7) REF DYNJ44249J, UDI/DI 40195327483020 (each), 10195327483029 (case), Lot Numbers:  23KBE536;  8) REF DYNJ44349L, UDI/DI 40195327394531 (each), 10195327394530 (case), Lot Numbers:  23KBD353;  9) REF DYNJ44349M, UDI/DI 40195327564378 (each), 10195327564377 (case), Lot Numbers:  24ABA446;  10) REF DYNJ53200C, UDI/DI 40193489779371 (each), 10193489779370 (case), Lot Numbers:  23KBC298;  11) REF DYNJ53270C, UDI/DI 40193489812566 (each), 10193489812565 (case), Lot Numbers:  23KBA462;  12) REF DYNJ54610A, UDI/DI 40195327456451 (each), 10195327456450 (case), Lot Numbers:  24ABD026;  13) REF DYNJ55255C, UDI/DI 40195327493753 (each), 10195327493752 (case), Lot Numbers:  23KBD956;  14) REF DYNJ58979, UDI/DI 40889942914938 (each), 10889942914937 (case), Lot Numbers:  24ABD861;  15) REF DYNJ62927, UDI/DI 40193489700245 (each), 10193489700244 (case), Lot Numbers:  23LBQ806;  16) REF DYNJ63190A, UDI/DI 40193489304603 (each), 10193489304602 (case), Lot Numbers:  23LBN122;  17) REF DYNJ66274A, UDI/DI 40195327151981 (each), 10195327151980 (case), Lot Numbers:  24ABB272;  18) REF DYNJ67109B, UDI/DI 40195327207084 (each), 10195327207083 (case), Lot Numbers:  24ABC426;  19) REF DYNJ68417C, UDI/DI 40195327341634 (each), 10195327341633 (case), Lot Numbers:  23KBC605;  20) REF DYNJ80227B, UDI/DI 40195327220144 (each), 10195327220143 (case), Lot Numbers:  24ABC423;  21) REF DYNJ80559A, UDI/DI 40195327512522 (each), 10195327512521 (case), Lot Numbers:  23LBP334;  22) REF DYNJ81880, UDI/DI 40195327153671 (each), 10195327153670 (case), Lot Numbers:  24ABE284;  23) REF DYNJ83158, UDI/DI 40195327236886 (each), 10195327236885 (case), Lot Numbers:  23LBU511;  24) REF DYNJ84083, UDI/DI 40195327332236 (each), 10195327332235 (case), Lot Numbers:  23LBL823;  25) REF DYNJ900289J, UDI/DI 40195327554034 (each), 10195327554033 (case), Lot Numbers:  24ABS131;  26) REF DYNJ900289J, UDI/DI 40195327554034 (each), 10195327554033 (case), Lot Numbers:  24ABE249;  27) REF DYNJ902626G, UDI/DI 40195327214334 (each), 10195327214333 (case), Lot Numbers:  24ABU280;  28) REF DYNJ903264A, UDI/DI 40889942632566 (each), 10889942632565 (case), Lot Numbers:  23LBF682;  29) REF DYNJ903428J, UDI/DI 40195327575060 (each), 10195327575069 (case), Lot Numbers:  24CBI692;  30) REF DYNJ903428J, UDI/DI 40195327575060 (each), 10195327575069 (case), Lot Numbers:  24ABS337;  31) REF DYNJ905769, UDI/DI 40193489507998 (each), 10193489507997 (case), Lot Numbers:  24ABS137;  32) REF DYNJ907056C, UDI/DI 40195327276875 (each), 10195327276874 (case), Lot Numbers:  24ABA207;  33) REF DYNJ908132, UDI/DI 40193489981521 (each), 10193489981520 (case), Lot Numbers:  24CBA800;  34) REF DYNJCH500, UDI/DI 40884389900421 (each), 10884389900420 (case), Lot Numbers:  23LBP611. 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": {
        "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-0160-2025&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-0160-2025&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-0160-2025/fda-classification",
      "@type": "schema:Claim",
      "name": "FDA classified recall Z-0160-2025 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
      },
      "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-0160-2025&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-0160-2025&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-0160-2025/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-0160-2025",
      "numberOfItems": 9,
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          "position": 1,
          "item": {
            "Field": "Recall number",
            "Value": "Z-0160-2025",
            "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"
          }
        },
        {
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          "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"
          }
        },
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          "position": 6,
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            "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"
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        },
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          "@type": "schema:ListItem",
          "position": 7,
          "item": {
            "Field": "Initiated",
            "Value": "2024-09-04",
            "Status": "recorded"
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          "position": 8,
          "item": {
            "Field": "Lot/code info",
            "Value": "1) REF CDS982091I, UDI/DI 40193489741644 (each), 10193489741643 (case), Lot Numbers:  24BBA623;  2) REF CDS984492B, UDI/DI 40193489637183 (each), 10193489637182 (case), Lot Numbers:  24ABB114;  3) REF DYNJ0798129I, UDI/DI 40195327226511 (each), 10195327226510 (case), Lot Numbers:  23KBB859;  4) REF DYNJ30591I, UDI/DI 40193489962841 (each), 10193489962840 (case), Lot Numbers:  24ABD228;  5) REF DYNJ37171A, UDI/DI 40884389750620 (each), 10884389750629 (case), Lot Numbers:  23KBD998;  6) REF DYNJ40836F, UDI/DI 40195327059539 (each), 10195327059538 (case), Lot Numbers:  23LBQ627;  7) REF DYNJ44249J, UDI/DI 40195327483020 (each), 10195327483029 (case), Lot Numbers:  23KBE536;  8) REF DYNJ44349L, UDI/DI 40195327394531 (each), 10195327394530 (case), Lot Numbers:  23KBD353;  9) REF DYNJ44349M, UDI/DI 40195327564378 (each), 10195327564377 (case), Lot Numbers:  24ABA446;  10) REF DYNJ53200C, UDI/DI 40193489779371 (each), 10193489779370 (case), Lot Numbers:  23KBC298;  11) REF DYNJ53270C, UDI/DI 40193489812566 (each), 10193489812565 (case), Lot Numbers:  23KBA462;  12) REF DYNJ54610A, UDI/DI 40195327456451 (each), 10195327456450 (case), Lot Numbers:  24ABD026;  13) REF DYNJ55255C, UDI/DI 40195327493753 (each), 10195327493752 (case), Lot Numbers:  23KBD956;  14) REF DYNJ58979, UDI/DI 40889942914938 (each), 10889942914937 (case), Lot Numbers:  24ABD861;  15) REF DYNJ62927, UDI/DI 40193489700245 (each), 10193489700244 (case), Lot Numbers:  23LBQ806;  16) REF DYNJ63190A, UDI/DI 40193489304603 (each), 10193489304602 (case), Lot Numbers:  23LBN122;  17) REF DYNJ66274A, UDI/DI 40195327151981 (each), 10195327151980 (case), Lot Numbers:  24ABB272;  18) REF DYNJ67109B, UDI/DI 40195327207084 (each), 10195327207083 (case), Lot Numbers:  24ABC426;  19) REF DYNJ68417C, UDI/DI 40195327341634 (each), 10195327341633 (case), Lot Numbers:  23KBC605;  20) REF DYNJ80227B, UDI/DI 40195327220144 (each), 10195327220143 (case), Lot Numbers:  24ABC423;  21) REF DYNJ80559A, UDI/DI 40195327512522 (each), 10195327512521 (case), Lot Numbers:  23LBP334;  22) REF DYNJ81880, UDI/DI 40195327153671 (each), 10195327153670 (case), Lot Numbers:  24ABE284;  23) REF DYNJ83158, UDI/DI 40195327236886 (each), 10195327236885 (case), Lot Numbers:  23LBU511;  24) REF DYNJ84083, UDI/DI 40195327332236 (each), 10195327332235 (case), Lot Numbers:  23LBL823;  25) REF DYNJ900289J, UDI/DI 40195327554034 (each), 10195327554033 (case), Lot Numbers:  24ABS131;  26) REF DYNJ900289J, UDI/DI 40195327554034 (each), 10195327554033 (case), Lot Numbers:  24ABE249;  27) REF DYNJ902626G, UDI/DI 40195327214334 (each), 10195327214333 (case), Lot Numbers:  24ABU280;  28) REF DYNJ903264A, UDI/DI 40889942632566 (each), 10889942632565 (case), Lot Numbers:  23LBF682;  29) REF DYNJ903428J, UDI/DI 40195327575060 (each), 10195327575069 (case), Lot Numbers:  24CBI692;  30) REF DYNJ903428J, UDI/DI 40195327575060 (each), 10195327575069 (case), Lot Numbers:  24ABS337;  31) REF DYNJ905769, UDI/DI 40193489507998 (each), 10193489507997 (case), Lot Numbers:  24ABS137;  32) REF DYNJ907056C, UDI/DI 40195327276875 (each), 10195327276874 (case), Lot Numbers:  24ABA207;  33) REF DYNJ908132, UDI/DI 40193489981521 (each), 10193489981520 (case), Lot Numbers:  24CBA800;  34) REF DYNJCH500, UDI/DI 40884389900421 (each), 10884389900420 (case), Lot Numbers:  23LBP611",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 9,
          "item": {
            "Field": "Distribution pattern",
            "Value": "Worldwide distribution - US Nationwide and the countries of Canada, Panama.",
            "Status": "recorded"
          }
        }
      ]
    }
  ]
}