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  "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-1617-2025.jsonld",
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  "name": "Medline Convenience kits used for various procedures:  1) BASIC CATARACT, Model Number: DYNJ41097A;   2) PK EYE, Model Number: DYNJ60631B;   3) CATARACT PACK, Model Number: DYNJ80316A;   4) BASIC EYE PACK, Model Number: DYNJ63707C;   5) EYE PACK WITH ACCESSORY PACK, Model Number: DYNJ85284;   6) PHACO PACK, Model Number: DYNJ44748I;   7) CAROMONT EYE TRAY-LF, Model Number: DYNJ17004L;   8) CHOG MINOR OPHTHALMIC PACK, Model Number: SYNJ10271B;   9) LIFESPAN VITRECTOMY PACK, Model Number: DYNJ80082;   10) DR KEYS EYE PACK 2, Model Number: DYNJ48256M;   11) VITRECTOMY PACK, Model Number: DYNJ55508B;   12) EYE PACK, Model Number: DYNJ63952A;   13) VITRECTOMY, Model Number: DYNJ67309C;   14) CATARACT PACK-MARY IMMACUL-LF, Model Number: DYNJ24516F;   15) DR FLOOD EYE PACK, Model Number: DYNJ57258G;   16) BLEPH PACK, Model Number: DYNJ67875;   17) CAROMONT EYE TRAY-LF, Model Number: DYNJ17004L;   18) EYE PLASTIC PACK, Model Number: DYNJ47859C;   19) OPHTHALMOLOGY PACK, Model Number: SYNJ10259A;   20) PLASTIC EYE, Model Number: DYNJ45667C;   21) BASIC EYE PACK, Model Number: DYNJ81548B;   22) WMC CATARACT PACK-LF, Model Number: DYNJ50653F;   23) BASIC CATARACT, Model Number: DYNJ41097A;   24) PK EYE, Model Number: DYNJ60631B;   25) EYE PLASTIC SURGERY PACK, Model Number: DYNJ44061;   26) CATARACT, Model Number: DYNJ44544F;   27) CATARACT PACK, Model Number: DYNJ49515D;   28) CATARACT PACK, Model Number: DYNJ35438F;   29) OPHTHALMIC PLASTIC PACK, Model Number: DYNJ55208A;   30) CATARACT PACK, Model Number: DYNJ81534B;   31) CATARACT PACK, Model Number: DYNJ49515D",
  "description": "FDA recall Z-1617-2025 — MEDLINE INDUSTRIES, LP - Northfield is recalling Medline Convenience kits used for various procedures:  1) BASIC CATARACT, Model Number: DYNJ41097A;   2) PK EYE, Model Number: DYNJ60631B;   3) CATARACT PACK, Model Number: DYNJ80316A;   4) BASIC EYE PACK, Model Number: DYNJ63707C;   5) EYE PACK WITH ACCESSORY PACK, Model Number: DYNJ85284;   6) PHACO PACK, Model Number: DYNJ44748I;   7) CAROMONT EYE TRAY-LF, Model Number: DYNJ17004L;   8) CHOG MINOR OPHTHALMIC PACK, Model Number: SYNJ10271B;   9) LIFESPAN VITRECTOMY PACK, Model Number: DYNJ80082;   10) DR KEYS EYE PACK 2, Model Number: DYNJ48256M;   11) VITRECTOMY PACK, Model Number: DYNJ55508B;   12) EYE PACK, Model Number: DYNJ63952A;   13) VITRECTOMY, Model Number: DYNJ67309C;   14) CATARACT PACK-MARY IMMACUL-LF, Model Number: DYNJ24516F;   15) DR FLOOD EYE PACK, Model Number: DYNJ57258G;   16) BLEPH PACK, Model Number: DYNJ67875;   17) CAROMONT EYE TRAY-LF, Model Number: DYNJ17004L;   18) EYE PLASTIC PACK, Model Number: DYNJ47859C;   19) OPHTHALMOLOGY PACK, Model Number: SYNJ10259A;   20) PLASTIC EYE, Model Number: DYNJ45667C;   21) BASIC EYE PACK, Model Number: DYNJ81548B;   22) WMC CATARACT PACK-LF, Model Number: DYNJ50653F;   23) BASIC CATARACT, Model Number: DYNJ41097A;   24) PK EYE, Model Number: DYNJ60631B;   25) EYE PLASTIC SURGERY PACK, Model Number: DYNJ44061;   26) CATARACT, Model Number: DYNJ44544F;   27) CATARACT PACK, Model Number: DYNJ49515D;   28) CATARACT PACK, Model Number: DYNJ35438F;   29) OPHTHALMIC PLASTIC PACK, Model Number: DYNJ55208A;   30) CATARACT PACK, Model Number: DYNJ81534B;   31) CATARACT PACK, Model Number: DYNJ49515D (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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    "name": "Medline Convenience kits used for various procedures:  1) BASIC CATARACT, Model Number: DYNJ41097A;   2) PK EYE, Model Number: DYNJ60631B;   3) CATARACT PACK, Model Number: DYNJ80316A;   4) BASIC EYE PACK, Model Number: DYNJ63707C;   5) EYE PACK WITH ACCESSORY PACK, Model Number: DYNJ85284;   6) PHACO PACK, Model Number: DYNJ44748I;   7) CAROMONT EYE TRAY-LF, Model Number: DYNJ17004L;   8) CHOG MINOR OPHTHALMIC PACK, Model Number: SYNJ10271B;   9) LIFESPAN VITRECTOMY PACK, Model Number: DYNJ80082;   10) DR KEYS EYE PACK 2, Model Number: DYNJ48256M;   11) VITRECTOMY PACK, Model Number: DYNJ55508B;   12) EYE PACK, Model Number: DYNJ63952A;   13) VITRECTOMY, Model Number: DYNJ67309C;   14) CATARACT PACK-MARY IMMACUL-LF, Model Number: DYNJ24516F;   15) DR FLOOD EYE PACK, Model Number: DYNJ57258G;   16) BLEPH PACK, Model Number: DYNJ67875;   17) CAROMONT EYE TRAY-LF, Model Number: DYNJ17004L;   18) EYE PLASTIC PACK, Model Number: DYNJ47859C;   19) OPHTHALMOLOGY PACK, Model Number: SYNJ10259A;   20) PLASTIC EYE, Model Number: DYNJ45667C;   21) BASIC EYE PACK, Model Number: DYNJ81548B;   22) WMC CATARACT PACK-LF, Model Number: DYNJ50653F;   23) BASIC CATARACT, Model Number: DYNJ41097A;   24) PK EYE, Model Number: DYNJ60631B;   25) EYE PLASTIC SURGERY PACK, Model Number: DYNJ44061;   26) CATARACT, Model Number: DYNJ44544F;   27) CATARACT PACK, Model Number: DYNJ49515D;   28) CATARACT PACK, Model Number: DYNJ35438F;   29) OPHTHALMIC PLASTIC PACK, Model Number: DYNJ55208A;   30) CATARACT PACK, Model Number: DYNJ81534B;   31) CATARACT PACK, Model Number: DYNJ49515D",
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      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-1617-2025/enforcement-record",
      "@type": "schema:Claim",
      "name": "FDA recall Z-1617-2025: MEDLINE INDUSTRIES, LP - Northfield is recalling Medline Convenience kits used for various procedures:  1) BASIC CATARACT, Model Number: DYNJ41097A;   2) PK EYE, Model Number: DYNJ60631B;   3) CATARACT PACK, Model Number: DYNJ80316A;   4) BASIC EYE PACK, Model Number: DYNJ63707C;   5) EYE PACK WITH ACCESSORY PACK, Model Number: DYNJ85284;   6) PHACO PACK, Model Number: DYNJ44748I;   7) CAROMONT EYE TRAY-LF, Model Number: DYNJ17004L;   8) CHOG MINOR OPHTHALMIC PACK, Model Number: SYNJ10271B;   9) LIFESPAN VITRECTOMY PACK, Model Number: DYNJ80082;   10) DR KEYS EYE PACK 2, Model Number: DYNJ48256M;   11) VITRECTOMY PACK, Model Number: DYNJ55508B;   12) EYE PACK, Model Number: DYNJ63952A;   13) VITRECTOMY, Model Number: DYNJ67309C;   14) CATARACT PACK-MARY IMMACUL-LF, Model Number: DYNJ24516F;   15) DR FLOOD EYE PACK, Model Number: DYNJ57258G;   16) BLEPH PACK, Model Number: DYNJ67875;   17) CAROMONT EYE TRAY-LF, Model Number: DYNJ17004L;   18) EYE PLASTIC PACK, Model Number: DYNJ47859C;   19) OPHTHALMOLOGY PACK, Model Number: SYNJ10259A;   20) PLASTIC EYE, Model Number: DYNJ45667C;   21) BASIC EYE PACK, Model Number: DYNJ81548B;   22) WMC CATARACT PACK-LF, Model Number: DYNJ50653F;   23) BASIC CATARACT, Model Number: DYNJ41097A;   24) PK EYE, Model Number: DYNJ60631B;   25) EYE PLASTIC SURGERY PACK, Model Number: DYNJ44061;   26) CATARACT, Model Number: DYNJ44544F;   27) CATARACT PACK, Model Number: DYNJ49515D;   28) CATARACT PACK, Model Number: DYNJ35438F;   29) OPHTHALMIC PLASTIC PACK, Model Number: DYNJ55208A;   30) CATARACT PACK, Model Number: DYNJ81534B;   31) CATARACT PACK, Model Number: DYNJ49515D",
      "text": "The FDA logged enforcement record Z-1617-2025: MEDLINE INDUSTRIES, LP - Northfield is voluntarily recalling Medline Convenience kits used for various procedures:  1) BASIC CATARACT, Model Number: DYNJ41097A;   2) PK EYE, Model Number: DYNJ60631B;   3) CATARACT PACK, Model Number: DYNJ80316A;   4) BASIC EYE PACK, Model Number: DYNJ63707C;   5) EYE PACK WITH ACCESSORY PACK, Model Number: DYNJ85284;   6) PHACO PACK, Model Number: DYNJ44748I;   7) CAROMONT EYE TRAY-LF, Model Number: DYNJ17004L;   8) CHOG MINOR OPHTHALMIC PACK, Model Number: SYNJ10271B;   9) LIFESPAN VITRECTOMY PACK, Model Number: DYNJ80082;   10) DR KEYS EYE PACK 2, Model Number: DYNJ48256M;   11) VITRECTOMY PACK, Model Number: DYNJ55508B;   12) EYE PACK, Model Number: DYNJ63952A;   13) VITRECTOMY, Model Number: DYNJ67309C;   14) CATARACT PACK-MARY IMMACUL-LF, Model Number: DYNJ24516F;   15) DR FLOOD EYE PACK, Model Number: DYNJ57258G;   16) BLEPH PACK, Model Number: DYNJ67875;   17) CAROMONT EYE TRAY-LF, Model Number: DYNJ17004L;   18) EYE PLASTIC PACK, Model Number: DYNJ47859C;   19) OPHTHALMOLOGY PACK, Model Number: SYNJ10259A;   20) PLASTIC EYE, Model Number: DYNJ45667C;   21) BASIC EYE PACK, Model Number: DYNJ81548B;   22) WMC CATARACT PACK-LF, Model Number: DYNJ50653F;   23) BASIC CATARACT, Model Number: DYNJ41097A;   24) PK EYE, Model Number: DYNJ60631B;   25) EYE PLASTIC SURGERY PACK, Model Number: DYNJ44061;   26) CATARACT, Model Number: DYNJ44544F;   27) CATARACT PACK, Model Number: DYNJ49515D;   28) CATARACT PACK, Model Number: DYNJ35438F;   29) OPHTHALMIC PLASTIC PACK, Model Number: DYNJ55208A;   30) CATARACT PACK, Model Number: DYNJ81534B;   31) CATARACT PACK, Model Number: DYNJ49515D — reason: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.. Status: Ongoing — the recall is still being carried out.. Initiated 2025-03-03. Affected lots/codes: 1) DYNJ41097A, UDI-DI: 10888277213487(each), 40888277213488(case), Lot Number: 24IBF244; 2) DYNJ60631B, UDI-DI: 10193489994421(each), 40193489994422(case), Lot Number: 24IBG352; 3) DYNJ80316A, UDI-DI: 10195327245221(each), 40195327245222(case), Lot Number: 24IBG593; 4) DYNJ63707C, UDI-DI: 10193489883503(each), 40193489883504(case), Lot Number: 24IBH027; 5) DYNJ85284, UDI-DI: 10195327486457(each), 40195327486458(case), Lot Number: 24IBH266; 6) DYNJ44748I, UDI-DI: 10193489273458(each), 40193489273459(case), Lot Number: 24IBH805; 7) DYNJ17004L, UDI-DI: 10193489244144(each), 40193489244145(case), Lot Number: 24IBS294; 8) SYNJ10271B, UDI-DI: 10193489457209(each), 40193489457200(case), Lot Number: 24IBS393; 9) DYNJ80082, UDI-DI: 10195327012007(each), 40195327012008(case), Lot Number: 24IBS417; 10) DYNJ48256M, UDI-DI: 10195327466176(each), 40195327466177(case), Lot Number: 24JBJ668; 11) DYNJ55508B, UDI-DI: 10195327266912(each), 40195327266913(case), Lot Number: 24JBN908; 12) DYNJ63952A, UDI-DI: 10193489393958(each), 40193489393959(case), Lot Number: 24JBT060; 13) DYNJ67309C, UDI-DI: 10195327668990(each), 40195327668991(case), Lot Number: 24JBT766; 14) DYNJ24516F, UDI-DI: 10195327278458(each), 40195327278459(case), Lot Number: 24JBU088; 15) DYNJ57258G, UDI-DI: 10195327491123(each), 40195327491124(case), Lot Number: 24JBV026; 16) DYNJ67875, UDI-DI: 10193489448825(each), 40193489448826(case), Lot Number: 24JBW137; 17) DYNJ17004L, UDI-DI: 10193489244144(each), 40193489244145(case), Lot Number: 24JBX679; 18) DYNJ47859C, UDI-DI: 10193489916065(each), 40193489916066(case), Lot Number: 24KBA576; 19) SYNJ10259A, UDI-DI: 10193489786873(each), 40193489786874(case), Lot Number: 24KBB063; 20) DYNJ45667C, UDI-DI: 10193489991062(each), 40193489991063(case), Lot Number: 24KBC142; 21) DYNJ81548B, UDI-DI: 10198459100277(each), 40198459100278(case), Lot Number: 24KBC156; 22) DYNJ50653F, UDI-DI: 10195327653149(each), 40195327653140(case), Lot Number: 24KBD242; 23) DYNJ41097A, UDI-DI: 10888277213487(each), 40888277213488(case), Lot Number: 24KBD377; 24) DYNJ60631B, UDI-DI: 10193489994421(each), 40193489994422(case), Lot Number: 24KBF041; 25) DYNJ44061, UDI-DI: 10888277081994(each), 40888277081995(case), Lot Number: 24KBF076; 26) DYNJ44544F, UDI-DI: 10198459122804(each), 40198459122805(case), Lot Number: 24KBF265; 27) DYNJ49515D, UDI-DI: 10193489508024(each), 40193489508025(case), Lot Number: 24KBH120; 28) DYNJ35438F, UDI-DI: 10193489612028(each), 40193489612029(case), Lot Number: 24KBH238; 29) DYNJ55208A, UDI-DI: 10193489967593(each), 40193489967594(case), Lot Number: 24KBH297; 30) DYNJ81534B, UDI-DI: 10198459082917(each), 40198459082918(case), Lot Number: 24KBH549; 31) DYNJ49515D, UDI-DI: 10193489508024(each), 40193489508025(case), Lot Number: 24KBI136. A RECORDED FDA enforcement action (occurred=true).",
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        "sourceUrl": "https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=Z-1617-2025&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-1617-2025&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-1617-2025/fda-classification",
      "@type": "schema:Claim",
      "name": "FDA classified recall Z-1617-2025 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,
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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-1617-2025&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-1617-2025&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-1617-2025/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-1617-2025",
      "numberOfItems": 9,
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          "position": 1,
          "item": {
            "Field": "Recall number",
            "Value": "Z-1617-2025",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 2,
          "item": {
            "Field": "Product type",
            "Value": "Devices",
            "Status": "recorded"
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        {
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          "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"
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          "@type": "schema:ListItem",
          "position": 5,
          "item": {
            "Field": "Recalling firm",
            "Value": "MEDLINE INDUSTRIES, LP - Northfield",
            "Status": "recorded"
          }
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          "@type": "schema:ListItem",
          "position": 6,
          "item": {
            "Field": "Reason",
            "Value": "There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.",
            "Status": "recorded"
          }
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        {
          "@type": "schema:ListItem",
          "position": 7,
          "item": {
            "Field": "Initiated",
            "Value": "2025-03-03",
            "Status": "recorded"
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          "item": {
            "Field": "Lot/code info",
            "Value": "1) DYNJ41097A, UDI-DI: 10888277213487(each), 40888277213488(case), Lot Number: 24IBF244; 2) DYNJ60631B, UDI-DI: 10193489994421(each), 40193489994422(case), Lot Number: 24IBG352; 3) DYNJ80316A, UDI-DI: 10195327245221(each), 40195327245222(case), Lot Number: 24IBG593; 4) DYNJ63707C, UDI-DI: 10193489883503(each), 40193489883504(case), Lot Number: 24IBH027; 5) DYNJ85284, UDI-DI: 10195327486457(each), 40195327486458(case), Lot Number: 24IBH266; 6) DYNJ44748I, UDI-DI: 10193489273458(each), 40193489273459(case), Lot Number: 24IBH805; 7) DYNJ17004L, UDI-DI: 10193489244144(each), 40193489244145(case), Lot Number: 24IBS294; 8) SYNJ10271B, UDI-DI: 10193489457209(each), 40193489457200(case), Lot Number: 24IBS393; 9) DYNJ80082, UDI-DI: 10195327012007(each), 40195327012008(case), Lot Number: 24IBS417; 10) DYNJ48256M, UDI-DI: 10195327466176(each), 40195327466177(case), Lot Number: 24JBJ668; 11) DYNJ55508B, UDI-DI: 10195327266912(each), 40195327266913(case), Lot Number: 24JBN908; 12) DYNJ63952A, UDI-DI: 10193489393958(each), 40193489393959(case), Lot Number: 24JBT060; 13) DYNJ67309C, UDI-DI: 10195327668990(each), 40195327668991(case), Lot Number: 24JBT766; 14) DYNJ24516F, UDI-DI: 10195327278458(each), 40195327278459(case), Lot Number: 24JBU088; 15) DYNJ57258G, UDI-DI: 10195327491123(each), 40195327491124(case), Lot Number: 24JBV026; 16) DYNJ67875, UDI-DI: 10193489448825(each), 40193489448826(case), Lot Number: 24JBW137; 17) DYNJ17004L, UDI-DI: 10193489244144(each), 40193489244145(case), Lot Number: 24JBX679; 18) DYNJ47859C, UDI-DI: 10193489916065(each), 40193489916066(case), Lot Number: 24KBA576; 19) SYNJ10259A, UDI-DI: 10193489786873(each), 40193489786874(case), Lot Number: 24KBB063; 20) DYNJ45667C, UDI-DI: 10193489991062(each), 40193489991063(case), Lot Number: 24KBC142; 21) DYNJ81548B, UDI-DI: 10198459100277(each), 40198459100278(case), Lot Number: 24KBC156; 22) DYNJ50653F, UDI-DI: 10195327653149(each), 40195327653140(case), Lot Number: 24KBD242; 23) DYNJ41097A, UDI-DI: 10888277213487(each), 40888277213488(case), Lot Number: 24KBD377; 24) DYNJ60631B, UDI-DI: 10193489994421(each), 40193489994422(case), Lot Number: 24KBF041; 25) DYNJ44061, UDI-DI: 10888277081994(each), 40888277081995(case), Lot Number: 24KBF076; 26) DYNJ44544F, UDI-DI: 10198459122804(each), 40198459122805(case), Lot Number: 24KBF265; 27) DYNJ49515D, UDI-DI: 10193489508024(each), 40193489508025(case), Lot Number: 24KBH120; 28) DYNJ35438F, UDI-DI: 10193489612028(each), 40193489612029(case), Lot Number: 24KBH238; 29) DYNJ55208A, UDI-DI: 10193489967593(each), 40193489967594(case), Lot Number: 24KBH297; 30) DYNJ81534B, UDI-DI: 10198459082917(each), 40198459082918(case), Lot Number: 24KBH549; 31) DYNJ49515D, UDI-DI: 10193489508024(each), 40193489508025(case), Lot Number: 24KBI136",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 9,
          "item": {
            "Field": "Distribution pattern",
            "Value": "Worldwide distribution - US Nationwide and the countries of Canada, Mexico, Panama, Virgin Islands.",
            "Status": "recorded"
          }
        }
      ]
    }
  ]
}