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  "name": "MEDLINE convenience kits labeled as:    1) LAKELAND SINGLE BASIN PACK-LF, REF DYNJ0619907I;   2) LAKELAND SINGLE BASIN PACK-LF, REF DYNJ0619907K;   3) LKLND SNGL BASIN PK RFID-LF, REF DYNJ0619907L;   4) BASIN SET W/ RING BASIN, REF DYNJ06966M;   5) OPEN HEART C--BASIN PACK-LF, REF DYNJ0867331G;   6) TOTAL KNEE BASIN B PACK-LF, REF DYNJ0867555L;   7) ST. ANNE'S MINOR BASIN PACK, REF DYNJ24622K;   8) ST. ANNE'S MAJOR BASIN SET UP, REF DYNJ24628M;   9) MAJOR BASIN SET, REF DYNJ41285B;   10) BASIN PACK, REF DYNJ50123D;   11) MAJOR BASIN TRAY, REF DYNJ54461F;   12) MAJOR BASIN TRAY, REF DYNJ54461G;   13) MAJOR BASIN TRAY, REF DYNJ54461I;   14) TR-MINOR KIT-LF, REF DYNJ54801F;   15) TR-MAJOR KIT-LF, REF DYNJ54802I;   16) MAJOR BASIN PACK, REF DYNJ59816A;   17) SINGLE BASIN PACK ST VINCENT, REF DYNJ60529D;   18) BASIN PACK, REF DYNJ60812B;   19) BASIN PACK SH, REF DYNJ60812C;   20) PLASTIC BASIN PACK, REF DYNJ63883C;   21) MINOR PACK, REF DYNJ63961D;   22) OSC BREAST PACK, REF DYNJ65808B;   23) OSC BASIN PACK, REF DYNJ68217A;   24) DELNOR VASCULAR BASIN PACK, REF DYNJ82257;   25) DELNOR BASIN PACK, REF DYNJ82267;   26) STAZ MAJOR BASIN, REF DYNJ909785;   27) LUMBAR, REF DYNJ909923",
  "description": "FDA recall Z-0634-2025 — MEDLINE INDUSTRIES, LP - Northfield is recalling MEDLINE convenience kits labeled as:    1) LAKELAND SINGLE BASIN PACK-LF, REF DYNJ0619907I;   2) LAKELAND SINGLE BASIN PACK-LF, REF DYNJ0619907K;   3) LKLND SNGL BASIN PK RFID-LF, REF DYNJ0619907L;   4) BASIN SET W/ RING BASIN, REF DYNJ06966M;   5) OPEN HEART C--BASIN PACK-LF, REF DYNJ0867331G;   6) TOTAL KNEE BASIN B PACK-LF, REF DYNJ0867555L;   7) ST. ANNE'S MINOR BASIN PACK, REF DYNJ24622K;   8) ST. ANNE'S MAJOR BASIN SET UP, REF DYNJ24628M;   9) MAJOR BASIN SET, REF DYNJ41285B;   10) BASIN PACK, REF DYNJ50123D;   11) MAJOR BASIN TRAY, REF DYNJ54461F;   12) MAJOR BASIN TRAY, REF DYNJ54461G;   13) MAJOR BASIN TRAY, REF DYNJ54461I;   14) TR-MINOR KIT-LF, REF DYNJ54801F;   15) TR-MAJOR KIT-LF, REF DYNJ54802I;   16) MAJOR BASIN PACK, REF DYNJ59816A;   17) SINGLE BASIN PACK ST VINCENT, REF DYNJ60529D;   18) BASIN PACK, REF DYNJ60812B;   19) BASIN PACK SH, REF DYNJ60812C;   20) PLASTIC BASIN PACK, REF DYNJ63883C;   21) MINOR PACK, REF DYNJ63961D;   22) OSC BREAST PACK, REF DYNJ65808B;   23) OSC BASIN PACK, REF DYNJ68217A;   24) DELNOR VASCULAR BASIN PACK, REF DYNJ82257;   25) DELNOR BASIN PACK, REF DYNJ82267;   26) STAZ MAJOR BASIN, REF DYNJ909785;   27) LUMBAR, REF DYNJ909923 (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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    "@type": "schema:MedicalDevice",
    "name": "MEDLINE convenience kits labeled as:    1) LAKELAND SINGLE BASIN PACK-LF, REF DYNJ0619907I;   2) LAKELAND SINGLE BASIN PACK-LF, REF DYNJ0619907K;   3) LKLND SNGL BASIN PK RFID-LF, REF DYNJ0619907L;   4) BASIN SET W/ RING BASIN, REF DYNJ06966M;   5) OPEN HEART C--BASIN PACK-LF, REF DYNJ0867331G;   6) TOTAL KNEE BASIN B PACK-LF, REF DYNJ0867555L;   7) ST. ANNE'S MINOR BASIN PACK, REF DYNJ24622K;   8) ST. ANNE'S MAJOR BASIN SET UP, REF DYNJ24628M;   9) MAJOR BASIN SET, REF DYNJ41285B;   10) BASIN PACK, REF DYNJ50123D;   11) MAJOR BASIN TRAY, REF DYNJ54461F;   12) MAJOR BASIN TRAY, REF DYNJ54461G;   13) MAJOR BASIN TRAY, REF DYNJ54461I;   14) TR-MINOR KIT-LF, REF DYNJ54801F;   15) TR-MAJOR KIT-LF, REF DYNJ54802I;   16) MAJOR BASIN PACK, REF DYNJ59816A;   17) SINGLE BASIN PACK ST VINCENT, REF DYNJ60529D;   18) BASIN PACK, REF DYNJ60812B;   19) BASIN PACK SH, REF DYNJ60812C;   20) PLASTIC BASIN PACK, REF DYNJ63883C;   21) MINOR PACK, REF DYNJ63961D;   22) OSC BREAST PACK, REF DYNJ65808B;   23) OSC BASIN PACK, REF DYNJ68217A;   24) DELNOR VASCULAR BASIN PACK, REF DYNJ82257;   25) DELNOR BASIN PACK, REF DYNJ82267;   26) STAZ MAJOR BASIN, REF DYNJ909785;   27) LUMBAR, REF DYNJ909923",
    "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-0634-2025/enforcement-record",
      "@type": "schema:Claim",
      "name": "FDA recall Z-0634-2025: MEDLINE INDUSTRIES, LP - Northfield is recalling MEDLINE convenience kits labeled as:    1) LAKELAND SINGLE BASIN PACK-LF, REF DYNJ0619907I;   2) LAKELAND SINGLE BASIN PACK-LF, REF DYNJ0619907K;   3) LKLND SNGL BASIN PK RFID-LF, REF DYNJ0619907L;   4) BASIN SET W/ RING BASIN, REF DYNJ06966M;   5) OPEN HEART C--BASIN PACK-LF, REF DYNJ0867331G;   6) TOTAL KNEE BASIN B PACK-LF, REF DYNJ0867555L;   7) ST. ANNE'S MINOR BASIN PACK, REF DYNJ24622K;   8) ST. ANNE'S MAJOR BASIN SET UP, REF DYNJ24628M;   9) MAJOR BASIN SET, REF DYNJ41285B;   10) BASIN PACK, REF DYNJ50123D;   11) MAJOR BASIN TRAY, REF DYNJ54461F;   12) MAJOR BASIN TRAY, REF DYNJ54461G;   13) MAJOR BASIN TRAY, REF DYNJ54461I;   14) TR-MINOR KIT-LF, REF DYNJ54801F;   15) TR-MAJOR KIT-LF, REF DYNJ54802I;   16) MAJOR BASIN PACK, REF DYNJ59816A;   17) SINGLE BASIN PACK ST VINCENT, REF DYNJ60529D;   18) BASIN PACK, REF DYNJ60812B;   19) BASIN PACK SH, REF DYNJ60812C;   20) PLASTIC BASIN PACK, REF DYNJ63883C;   21) MINOR PACK, REF DYNJ63961D;   22) OSC BREAST PACK, REF DYNJ65808B;   23) OSC BASIN PACK, REF DYNJ68217A;   24) DELNOR VASCULAR BASIN PACK, REF DYNJ82257;   25) DELNOR BASIN PACK, REF DYNJ82267;   26) STAZ MAJOR BASIN, REF DYNJ909785;   27) LUMBAR, REF DYNJ909923",
      "text": "The FDA logged enforcement record Z-0634-2025: MEDLINE INDUSTRIES, LP - Northfield is voluntarily recalling MEDLINE convenience kits labeled as:    1) LAKELAND SINGLE BASIN PACK-LF, REF DYNJ0619907I;   2) LAKELAND SINGLE BASIN PACK-LF, REF DYNJ0619907K;   3) LKLND SNGL BASIN PK RFID-LF, REF DYNJ0619907L;   4) BASIN SET W/ RING BASIN, REF DYNJ06966M;   5) OPEN HEART C--BASIN PACK-LF, REF DYNJ0867331G;   6) TOTAL KNEE BASIN B PACK-LF, REF DYNJ0867555L;   7) ST. ANNE'S MINOR BASIN PACK, REF DYNJ24622K;   8) ST. ANNE'S MAJOR BASIN SET UP, REF DYNJ24628M;   9) MAJOR BASIN SET, REF DYNJ41285B;   10) BASIN PACK, REF DYNJ50123D;   11) MAJOR BASIN TRAY, REF DYNJ54461F;   12) MAJOR BASIN TRAY, REF DYNJ54461G;   13) MAJOR BASIN TRAY, REF DYNJ54461I;   14) TR-MINOR KIT-LF, REF DYNJ54801F;   15) TR-MAJOR KIT-LF, REF DYNJ54802I;   16) MAJOR BASIN PACK, REF DYNJ59816A;   17) SINGLE BASIN PACK ST VINCENT, REF DYNJ60529D;   18) BASIN PACK, REF DYNJ60812B;   19) BASIN PACK SH, REF DYNJ60812C;   20) PLASTIC BASIN PACK, REF DYNJ63883C;   21) MINOR PACK, REF DYNJ63961D;   22) OSC BREAST PACK, REF DYNJ65808B;   23) OSC BASIN PACK, REF DYNJ68217A;   24) DELNOR VASCULAR BASIN PACK, REF DYNJ82257;   25) DELNOR BASIN PACK, REF DYNJ82267;   26) STAZ MAJOR BASIN, REF DYNJ909785;   27) LUMBAR, REF DYNJ909923 — reason: Medline is recalling medical convenience manufactured using certain lots of SafeAir Smoke Evacuation Pencil which were subsequently recalled by Stryker.. Status: Ongoing — the recall is still being carried out.. Initiated 2024-10-09. Affected lots/codes: 1) REF DYNJ0619907I, UDI/DI 10195327239480 (each) 40195327239481 (case), Lot Numbers:  22IMG033;   2) REF DYNJ0619907K, UDI/DI 10195327295905 (each) 40195327295906 (case), Lot Numbers: 22LME111;    3) REF DYNJ0619907L, UDI/DI 10195327333119 (each) 40195327333110 (case), Lot Numbers:   23JBH171, 23HBV761, 23FMI052;   4) REF DYNJ06966M, UDI/DI 10195327349059 (each) 40195327349050 (case), Lot Numbers:   23EBR799, 23IBI141, 23KBC445, 23LBJ670;   5) REF DYNJ0867331G, UDI/DI 10195327118433 (each) 40195327118434 (case), Lot Numbers:   22EDA376, 22FDA407;   6) REF DYNJ0867555L, UDI/DI 10195327202613 (each) 40195327202614 (case), Lot Numbers:   23DDB147;   7) REF DYNJ24622K, UDI/DI 10195327109127 (each) 40195327109128 (case), Lot Numbers:   23ABN514, 22EBS282, 22EBE400, 23CBV810, 23CBH097, 23EBT659;   8) REF DYNJ24628M, UDI/DI 10195327109134 (each) 40195327109135 (case), Lot Numbers:   22FLA375, 22DLA993, 22ILA590, 23GLA918, 23FLA366, 23DLA800, 23BLA536, 22JLA323, 23CLB087;   9) REF DYNJ41285B, UDI/DI 10195327515546 (each) 40195327515547 (case), Lot Numbers:   23KBF131;   10) REF DYNJ50123D, UDI/DI 10195327201999 (each) 40195327201990 (case), Lot Numbers:   22KBI121, 22KBI122, 23CBT112, 23EBB417;   11) REF DYNJ54461F, UDI/DI 10195327155728 (each) 40195327155729 (case), Lot Numbers:   22IMA730, 22LMG820, 23EMB339, 23DMD912, 23HMG790, 23HMC613, 23GMF360, 23IMH847;   12) REF DYNJ54461G, UDI/DI 10195327543570 (each) 40195327543571 (case), Lot Numbers:   23KMA747, 23KBS302, 24ABI360;   13) REF DYNJ54461I, UDI/DI 10195327613730 (each) 40195327613731 (case), Lot Numbers:   24BBG122, 24ABS064, 24DBG019;   14) REF DYNJ54801F, UDI/DI 10195327450861 (each) 40195327450862 (case), Lot Numbers:   23HDC012;   15) REF DYNJ54802I, UDI/DI 10195327450878 (each) 40195327450879 (case), Lot Numbers:   23FDC386, 23IDA377;   16) REF DYNJ59816A, UDI/DI 10195327331573 (each) 40195327331574 (case), Lot Numbers:   23CBV819, 23EBF888;   17) REF DYNJ60529D, UDI/DI 10195327523411 (each) 40195327523412 (case), Lot Numbers:   23JMH503;   18) REF DYNJ60812B, UDI/DI 10195327454630 (each) 40195327454631 (case), Lot Numbers:   23HBL174;   19) REF DYNJ60812C, UDI/DI 10195327521226 (each) 40195327521227 (case), Lot Numbers:   23KBE930, 23JBN323, 23LBN436;   20) REF DYNJ63883C, UDI/DI 10195327221829 (each) 40195327221820 (case), Lot Numbers:   23IDA838, 23GDA969, 23ADA553, 22JDC142, 23KDA710, 24ADB347, 23CDB848, 23EDA013, 24CDA880;   21) REF DYNJ63961D, UDI/DI 10195327428877 (each) 40195327428878 (case), Lot Numbers:   23HDC162, 23GDB814, 23JDA825, 24BDA028, 24DDA624;   22) REF DYNJ65808B, UDI/DI 10195327273552 (each) 40195327273553 (case), Lot Numbers:   23AMI184, 23AMA558;   23) REF DYNJ68217A, UDI/DI 10195327352523 (each) 40195327352524 (case), Lot Numbers:   23CME053, 23FMG407;   24) REF DYNJ82257, UDI/DI 10195327181659 (each) 40195327181650 (case), Lot Numbers:   23IMA316;   25) REF DYNJ82267, UDI/DI 10195327182229 (each) 40195327182220 (case), Lot Numbers:   23GDB214, 23IDC201;   26) REF DYNJ909785, UDI/DI 10195327475819 (each) 40195327475810 (case), Lot Numbers:   23HBU592, 23IBN694;   27) REF DYNJ909923, UDI/DI 10195327504533 (each) 40195327504534 (case), Lot Numbers:  23LMB294, 24BMC919. A RECORDED FDA enforcement action (occurred=true).",
      "claimType": "official_fact",
      "reviewStatus": "current",
      "commercialInfluence": false,
      "epistemicStatus": {
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        "operative": 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-0634-2025&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-0634-2025&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-0634-2025/fda-classification",
      "@type": "schema:Claim",
      "name": "FDA classified recall Z-0634-2025 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-0634-2025&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-0634-2025&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-0634-2025/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-0634-2025",
      "numberOfItems": 9,
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          "@type": "schema:ListItem",
          "position": 1,
          "item": {
            "Field": "Recall number",
            "Value": "Z-0634-2025",
            "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": "Medline is recalling medical convenience manufactured using certain lots of SafeAir Smoke Evacuation Pencil which were subsequently recalled by Stryker.",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 7,
          "item": {
            "Field": "Initiated",
            "Value": "2024-10-09",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 8,
          "item": {
            "Field": "Lot/code info",
            "Value": "1) REF DYNJ0619907I, UDI/DI 10195327239480 (each) 40195327239481 (case), Lot Numbers:  22IMG033;   2) REF DYNJ0619907K, UDI/DI 10195327295905 (each) 40195327295906 (case), Lot Numbers: 22LME111;    3) REF DYNJ0619907L, UDI/DI 10195327333119 (each) 40195327333110 (case), Lot Numbers:   23JBH171, 23HBV761, 23FMI052;   4) REF DYNJ06966M, UDI/DI 10195327349059 (each) 40195327349050 (case), Lot Numbers:   23EBR799, 23IBI141, 23KBC445, 23LBJ670;   5) REF DYNJ0867331G, UDI/DI 10195327118433 (each) 40195327118434 (case), Lot Numbers:   22EDA376, 22FDA407;   6) REF DYNJ0867555L, UDI/DI 10195327202613 (each) 40195327202614 (case), Lot Numbers:   23DDB147;   7) REF DYNJ24622K, UDI/DI 10195327109127 (each) 40195327109128 (case), Lot Numbers:   23ABN514, 22EBS282, 22EBE400, 23CBV810, 23CBH097, 23EBT659;   8) REF DYNJ24628M, UDI/DI 10195327109134 (each) 40195327109135 (case), Lot Numbers:   22FLA375, 22DLA993, 22ILA590, 23GLA918, 23FLA366, 23DLA800, 23BLA536, 22JLA323, 23CLB087;   9) REF DYNJ41285B, UDI/DI 10195327515546 (each) 40195327515547 (case), Lot Numbers:   23KBF131;   10) REF DYNJ50123D, UDI/DI 10195327201999 (each) 40195327201990 (case), Lot Numbers:   22KBI121, 22KBI122, 23CBT112, 23EBB417;   11) REF DYNJ54461F, UDI/DI 10195327155728 (each) 40195327155729 (case), Lot Numbers:   22IMA730, 22LMG820, 23EMB339, 23DMD912, 23HMG790, 23HMC613, 23GMF360, 23IMH847;   12) REF DYNJ54461G, UDI/DI 10195327543570 (each) 40195327543571 (case), Lot Numbers:   23KMA747, 23KBS302, 24ABI360;   13) REF DYNJ54461I, UDI/DI 10195327613730 (each) 40195327613731 (case), Lot Numbers:   24BBG122, 24ABS064, 24DBG019;   14) REF DYNJ54801F, UDI/DI 10195327450861 (each) 40195327450862 (case), Lot Numbers:   23HDC012;   15) REF DYNJ54802I, UDI/DI 10195327450878 (each) 40195327450879 (case), Lot Numbers:   23FDC386, 23IDA377;   16) REF DYNJ59816A, UDI/DI 10195327331573 (each) 40195327331574 (case), Lot Numbers:   23CBV819, 23EBF888;   17) REF DYNJ60529D, UDI/DI 10195327523411 (each) 40195327523412 (case), Lot Numbers:   23JMH503;   18) REF DYNJ60812B, UDI/DI 10195327454630 (each) 40195327454631 (case), Lot Numbers:   23HBL174;   19) REF DYNJ60812C, UDI/DI 10195327521226 (each) 40195327521227 (case), Lot Numbers:   23KBE930, 23JBN323, 23LBN436;   20) REF DYNJ63883C, UDI/DI 10195327221829 (each) 40195327221820 (case), Lot Numbers:   23IDA838, 23GDA969, 23ADA553, 22JDC142, 23KDA710, 24ADB347, 23CDB848, 23EDA013, 24CDA880;   21) REF DYNJ63961D, UDI/DI 10195327428877 (each) 40195327428878 (case), Lot Numbers:   23HDC162, 23GDB814, 23JDA825, 24BDA028, 24DDA624;   22) REF DYNJ65808B, UDI/DI 10195327273552 (each) 40195327273553 (case), Lot Numbers:   23AMI184, 23AMA558;   23) REF DYNJ68217A, UDI/DI 10195327352523 (each) 40195327352524 (case), Lot Numbers:   23CME053, 23FMG407;   24) REF DYNJ82257, UDI/DI 10195327181659 (each) 40195327181650 (case), Lot Numbers:   23IMA316;   25) REF DYNJ82267, UDI/DI 10195327182229 (each) 40195327182220 (case), Lot Numbers:   23GDB214, 23IDC201;   26) REF DYNJ909785, UDI/DI 10195327475819 (each) 40195327475810 (case), Lot Numbers:   23HBU592, 23IBN694;   27) REF DYNJ909923, UDI/DI 10195327504533 (each) 40195327504534 (case), Lot Numbers:  23LMB294, 24BMC919",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 9,
          "item": {
            "Field": "Distribution pattern",
            "Value": "US Nationwide distribution.",
            "Status": "recorded"
          }
        }
      ]
    }
  ]
}