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  "name": "Medline brand medical procedure convenience kits, labeled as:    1) CYSTO CDS, REF CDS983525D;   2) CYSTO CDS, REF CDS983525D;   3) CYSTO PACK-LF, REF DYNJ25834B;   4) CYSTO PACK, REF DYNJ35569C;   5) PAVILION MINOR PACK, REF DYNJ40724D;   6) CYSTOSCOPY PACK, REF DYNJ41105C;   7) MINOR PACK, REF DYNJ42132A;   8) RECTAL PRONE PACK, REF DYNJ43380A;   9) HERNIA APPENDECTOMY TEGH-LF, REF DYNJ46716;   10) CYSTO PACK, REF DYNJ47821F;   11) CYSTO PACK, REF DYNJ48978C;   12) CYSTO PACK, REF DYNJ50428C;   13) MID HUDSON CYSTO PACK, REF DYNJ53418B;   14) CYSTO PACK-LF, REF DYNJ55479D;   15) CYSTO PACK, REF DYNJ58445A;   16) MINOR PACK, REF DYNJ58566B;   17) CSTM PK GEN NEW ENGL SURG, REF DYNJ59431;   18) RIDGEWOOD LAP PACK-LF, REF DYNJ60077A;   19) FLEXIBLE CYS PACK, REF DYNJ62111C;   20) CYSTO PACK, REF DYNJ65830A;   21) MAIN & ODS CYSTO PACK, REF DYNJ66821A;   22) PROCEDURE CYSTO PACK, REF DYNJ68883;   23) CYSTO PACK, REF DYNJ69729;   24) MINOR SURGERY PACK, REF DYNJ80004;   25) LAPAROSCOPY PACK, REF DYNJ80763;   26) LAPAROSCOPY PACK, REF DYNJ80763;   27) CYSTO PACK, REF DYNJ82626;   28) MINOR PACK, REF DYNJ83155;   29) SY CYSTO, REF DYNJ900583M;   30) CYSTO, REF DYNJ905569B;   31) CYSTO, REF DYNJ907541A;   32) SET UP PACK-LF, REF LLSCASET01;   33) MAJOR PACK, REF SYNJ910011B",
  "description": "FDA recall Z-0161-2025 — MEDLINE INDUSTRIES, LP - Northfield is recalling Medline brand medical procedure convenience kits, labeled as:    1) CYSTO CDS, REF CDS983525D;   2) CYSTO CDS, REF CDS983525D;   3) CYSTO PACK-LF, REF DYNJ25834B;   4) CYSTO PACK, REF DYNJ35569C;   5) PAVILION MINOR PACK, REF DYNJ40724D;   6) CYSTOSCOPY PACK, REF DYNJ41105C;   7) MINOR PACK, REF DYNJ42132A;   8) RECTAL PRONE PACK, REF DYNJ43380A;   9) HERNIA APPENDECTOMY TEGH-LF, REF DYNJ46716;   10) CYSTO PACK, REF DYNJ47821F;   11) CYSTO PACK, REF DYNJ48978C;   12) CYSTO PACK, REF DYNJ50428C;   13) MID HUDSON CYSTO PACK, REF DYNJ53418B;   14) CYSTO PACK-LF, REF DYNJ55479D;   15) CYSTO PACK, REF DYNJ58445A;   16) MINOR PACK, REF DYNJ58566B;   17) CSTM PK GEN NEW ENGL SURG, REF DYNJ59431;   18) RIDGEWOOD LAP PACK-LF, REF DYNJ60077A;   19) FLEXIBLE CYS PACK, REF DYNJ62111C;   20) CYSTO PACK, REF DYNJ65830A;   21) MAIN & ODS CYSTO PACK, REF DYNJ66821A;   22) PROCEDURE CYSTO PACK, REF DYNJ68883;   23) CYSTO PACK, REF DYNJ69729;   24) MINOR SURGERY PACK, REF DYNJ80004;   25) LAPAROSCOPY PACK, REF DYNJ80763;   26) LAPAROSCOPY PACK, REF DYNJ80763;   27) CYSTO PACK, REF DYNJ82626;   28) MINOR PACK, REF DYNJ83155;   29) SY CYSTO, REF DYNJ900583M;   30) CYSTO, REF DYNJ905569B;   31) CYSTO, REF DYNJ907541A;   32) SET UP PACK-LF, REF LLSCASET01;   33) MAJOR PACK, REF SYNJ910011B (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) CYSTO CDS, REF CDS983525D;   2) CYSTO CDS, REF CDS983525D;   3) CYSTO PACK-LF, REF DYNJ25834B;   4) CYSTO PACK, REF DYNJ35569C;   5) PAVILION MINOR PACK, REF DYNJ40724D;   6) CYSTOSCOPY PACK, REF DYNJ41105C;   7) MINOR PACK, REF DYNJ42132A;   8) RECTAL PRONE PACK, REF DYNJ43380A;   9) HERNIA APPENDECTOMY TEGH-LF, REF DYNJ46716;   10) CYSTO PACK, REF DYNJ47821F;   11) CYSTO PACK, REF DYNJ48978C;   12) CYSTO PACK, REF DYNJ50428C;   13) MID HUDSON CYSTO PACK, REF DYNJ53418B;   14) CYSTO PACK-LF, REF DYNJ55479D;   15) CYSTO PACK, REF DYNJ58445A;   16) MINOR PACK, REF DYNJ58566B;   17) CSTM PK GEN NEW ENGL SURG, REF DYNJ59431;   18) RIDGEWOOD LAP PACK-LF, REF DYNJ60077A;   19) FLEXIBLE CYS PACK, REF DYNJ62111C;   20) CYSTO PACK, REF DYNJ65830A;   21) MAIN & ODS CYSTO PACK, REF DYNJ66821A;   22) PROCEDURE CYSTO PACK, REF DYNJ68883;   23) CYSTO PACK, REF DYNJ69729;   24) MINOR SURGERY PACK, REF DYNJ80004;   25) LAPAROSCOPY PACK, REF DYNJ80763;   26) LAPAROSCOPY PACK, REF DYNJ80763;   27) CYSTO PACK, REF DYNJ82626;   28) MINOR PACK, REF DYNJ83155;   29) SY CYSTO, REF DYNJ900583M;   30) CYSTO, REF DYNJ905569B;   31) CYSTO, REF DYNJ907541A;   32) SET UP PACK-LF, REF LLSCASET01;   33) MAJOR PACK, REF SYNJ910011B",
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      "name": "MEDLINE INDUSTRIES, LP - Northfield"
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    {
      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-0161-2025/enforcement-record",
      "@type": "schema:Claim",
      "name": "FDA recall Z-0161-2025: MEDLINE INDUSTRIES, LP - Northfield is recalling Medline brand medical procedure convenience kits, labeled as:    1) CYSTO CDS, REF CDS983525D;   2) CYSTO CDS, REF CDS983525D;   3) CYSTO PACK-LF, REF DYNJ25834B;   4) CYSTO PACK, REF DYNJ35569C;   5) PAVILION MINOR PACK, REF DYNJ40724D;   6) CYSTOSCOPY PACK, REF DYNJ41105C;   7) MINOR PACK, REF DYNJ42132A;   8) RECTAL PRONE PACK, REF DYNJ43380A;   9) HERNIA APPENDECTOMY TEGH-LF, REF DYNJ46716;   10) CYSTO PACK, REF DYNJ47821F;   11) CYSTO PACK, REF DYNJ48978C;   12) CYSTO PACK, REF DYNJ50428C;   13) MID HUDSON CYSTO PACK, REF DYNJ53418B;   14) CYSTO PACK-LF, REF DYNJ55479D;   15) CYSTO PACK, REF DYNJ58445A;   16) MINOR PACK, REF DYNJ58566B;   17) CSTM PK GEN NEW ENGL SURG, REF DYNJ59431;   18) RIDGEWOOD LAP PACK-LF, REF DYNJ60077A;   19) FLEXIBLE CYS PACK, REF DYNJ62111C;   20) CYSTO PACK, REF DYNJ65830A;   21) MAIN & ODS CYSTO PACK, REF DYNJ66821A;   22) PROCEDURE CYSTO PACK, REF DYNJ68883;   23) CYSTO PACK, REF DYNJ69729;   24) MINOR SURGERY PACK, REF DYNJ80004;   25) LAPAROSCOPY PACK, REF DYNJ80763;   26) LAPAROSCOPY PACK, REF DYNJ80763;   27) CYSTO PACK, REF DYNJ82626;   28) MINOR PACK, REF DYNJ83155;   29) SY CYSTO, REF DYNJ900583M;   30) CYSTO, REF DYNJ905569B;   31) CYSTO, REF DYNJ907541A;   32) SET UP PACK-LF, REF LLSCASET01;   33) MAJOR PACK, REF SYNJ910011B",
      "text": "The FDA logged enforcement record Z-0161-2025: MEDLINE INDUSTRIES, LP - Northfield is voluntarily recalling Medline brand medical procedure convenience kits, labeled as:    1) CYSTO CDS, REF CDS983525D;   2) CYSTO CDS, REF CDS983525D;   3) CYSTO PACK-LF, REF DYNJ25834B;   4) CYSTO PACK, REF DYNJ35569C;   5) PAVILION MINOR PACK, REF DYNJ40724D;   6) CYSTOSCOPY PACK, REF DYNJ41105C;   7) MINOR PACK, REF DYNJ42132A;   8) RECTAL PRONE PACK, REF DYNJ43380A;   9) HERNIA APPENDECTOMY TEGH-LF, REF DYNJ46716;   10) CYSTO PACK, REF DYNJ47821F;   11) CYSTO PACK, REF DYNJ48978C;   12) CYSTO PACK, REF DYNJ50428C;   13) MID HUDSON CYSTO PACK, REF DYNJ53418B;   14) CYSTO PACK-LF, REF DYNJ55479D;   15) CYSTO PACK, REF DYNJ58445A;   16) MINOR PACK, REF DYNJ58566B;   17) CSTM PK GEN NEW ENGL SURG, REF DYNJ59431;   18) RIDGEWOOD LAP PACK-LF, REF DYNJ60077A;   19) FLEXIBLE CYS PACK, REF DYNJ62111C;   20) CYSTO PACK, REF DYNJ65830A;   21) MAIN & ODS CYSTO PACK, REF DYNJ66821A;   22) PROCEDURE CYSTO PACK, REF DYNJ68883;   23) CYSTO PACK, REF DYNJ69729;   24) MINOR SURGERY PACK, REF DYNJ80004;   25) LAPAROSCOPY PACK, REF DYNJ80763;   26) LAPAROSCOPY PACK, REF DYNJ80763;   27) CYSTO PACK, REF DYNJ82626;   28) MINOR PACK, REF DYNJ83155;   29) SY CYSTO, REF DYNJ900583M;   30) CYSTO, REF DYNJ905569B;   31) CYSTO, REF DYNJ907541A;   32) SET UP PACK-LF, REF LLSCASET01;   33) MAJOR PACK, REF SYNJ910011B — 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 CDS983525D, UDI/DI 40195327429905 (each) 10195327429904 (case), Lot Numbers:  24ABW238;  2) REF CDS983525D, UDI/DI 40195327429905 (each) 10195327429904 (case), Lot Numbers:  23KBU714;  3) REF DYNJ25834B, UDI/DI 40193489849555 (each) 10193489849554 (case), Lot Numbers:  24ABG332;  4) REF DYNJ35569C, UDI/DI 40195327498253 (each) 10195327498252 (case), Lot Numbers:  23LBL736;  5) REF DYNJ40724D, UDI/DI 40195327420773 (each) 10195327420772 (case), Lot Numbers:  24ABG713;  6) REF DYNJ41105C, UDI/DI 40193489969659 (each) 10193489969658 (case), Lot Numbers:  24ABA628;  7) REF DYNJ42132A, UDI/DI 40195327385270 (each) 10195327385279 (case), Lot Numbers:  23LBS108;  8) REF DYNJ43380A, UDI/DI 40888277265913 (each) 10888277265912 (case), Lot Numbers:  23KBD028;  9) REF DYNJ46716, UDI/DI 40888277597069 (each) 10888277597068 (case), Lot Numbers:  23LBM976;  10) REF DYNJ47821F, UDI/DI 40193489956796 (each) 10193489956795 (case), Lot Numbers:  24ABC507;  11) REF DYNJ48978C, UDI/DI 40195327325948 (each) 10195327325947 (case), Lot Numbers:  23LBP883;  12) REF DYNJ50428C, UDI/DI 40195327504039 (each) 10195327504038 (case), Lot Numbers:  23LBN301;  13) REF DYNJ53418B, UDI/DI 40195327372270 (each) 10195327372279 (case), Lot Numbers:  23LBO773;  14) REF DYNJ55479D, UDI/DI 40195327416769 (each) 10195327416768 (case), Lot Numbers:  23LBL444;  15) REF DYNJ58445A, UDI/DI 40195327585953 (each) 10195327585952 (case), Lot Numbers:  23LBU911;  16) REF DYNJ58566B, UDI/DI 40195327243228 (each) 10195327243227 (case), Lot Numbers:  23KBC919;  17) REF DYNJ59431, UDI/DI 40888277741257 (each) 10888277741256 (case), Lot Numbers:  24ABG210;  18) REF DYNJ60077A, UDI/DI 40193489862905 (each) 10193489862904 (case), Lot Numbers:  23LBO542;  19) REF DYNJ62111C, UDI/DI 40195327312146 (each) 10195327312145 (case), Lot Numbers:  23LBP204;  20) REF DYNJ65830A, UDI/DI 40195327588732 (each) 10195327588731 (case), Lot Numbers:  23LBR366;  21) REF DYNJ66821A, UDI/DI 40193489974929 (each) 10193489974928 (case), Lot Numbers:  23KBQ852;  22) REF DYNJ68883, UDI/DI 40193489848329 (each) 10193489848328 (case), Lot Numbers:  23KBC527;  23) REF DYNJ69729, UDI/DI 40193489973267 (each) 10193489973266 (case), Lot Numbers:  24ABD664;  24) REF DYNJ80004, UDI/DI 40195327005192 (each) 10195327005191 (case), Lot Numbers:  23LBP094;  25) REF DYNJ80763, UDI/DI 40195327076611 (each) 10195327076610 (case), Lot Numbers:  24ABG464;  26) REF DYNJ80763, UDI/DI 40195327076611 (each) 10195327076610 (case), Lot Numbers:  23LBU050;  27) REF DYNJ82626, UDI/DI 40195327199488 (each) 10195327199487 (case), Lot Numbers:  24ABN216;  28) REF DYNJ83155, UDI/DI 40195327236855 (each) 10195327236854 (case), Lot Numbers:  23LBV474;  29) REF DYNJ900583M, UDI/DI 40195327061853 (each) 10195327061852 (case), Lot Numbers:  24ABU214;  30) REF DYNJ905569B, UDI/DI 40193489995672 (each) 10193489995671 (case), Lot Numbers:  24ABJ966;  31) REF DYNJ907541A, UDI/DI 40195327054268 (each) 10195327054267 (case), Lot Numbers:  23KBT202;  32) REF LLSCASET01, UDI/DI 40080196120681 (each) 10080196120680 (case), Lot Numbers:  23LBM079;  33) REF SYNJ910011B, UDI/DI 40195327246809 (each) 10195327246808 (case), Lot Numbers:  24ABS212. 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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        "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-0161-2025&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-0161-2025&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-0161-2025/fda-classification",
      "@type": "schema:Claim",
      "name": "FDA classified recall Z-0161-2025 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-0161-2025&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-0161-2025&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-0161-2025/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-0161-2025",
      "numberOfItems": 9,
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          "position": 1,
          "item": {
            "Field": "Recall number",
            "Value": "Z-0161-2025",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 2,
          "item": {
            "Field": "Product type",
            "Value": "Devices",
            "Status": "recorded"
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        },
        {
          "@type": "schema:ListItem",
          "position": 3,
          "item": {
            "Field": "Classification",
            "Value": "Class II",
            "Status": "determination"
          }
        },
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          "@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"
          }
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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",
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          "item": {
            "Field": "Initiated",
            "Value": "2024-09-04",
            "Status": "recorded"
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          "item": {
            "Field": "Lot/code info",
            "Value": "1) REF CDS983525D, UDI/DI 40195327429905 (each) 10195327429904 (case), Lot Numbers:  24ABW238;  2) REF CDS983525D, UDI/DI 40195327429905 (each) 10195327429904 (case), Lot Numbers:  23KBU714;  3) REF DYNJ25834B, UDI/DI 40193489849555 (each) 10193489849554 (case), Lot Numbers:  24ABG332;  4) REF DYNJ35569C, UDI/DI 40195327498253 (each) 10195327498252 (case), Lot Numbers:  23LBL736;  5) REF DYNJ40724D, UDI/DI 40195327420773 (each) 10195327420772 (case), Lot Numbers:  24ABG713;  6) REF DYNJ41105C, UDI/DI 40193489969659 (each) 10193489969658 (case), Lot Numbers:  24ABA628;  7) REF DYNJ42132A, UDI/DI 40195327385270 (each) 10195327385279 (case), Lot Numbers:  23LBS108;  8) REF DYNJ43380A, UDI/DI 40888277265913 (each) 10888277265912 (case), Lot Numbers:  23KBD028;  9) REF DYNJ46716, UDI/DI 40888277597069 (each) 10888277597068 (case), Lot Numbers:  23LBM976;  10) REF DYNJ47821F, UDI/DI 40193489956796 (each) 10193489956795 (case), Lot Numbers:  24ABC507;  11) REF DYNJ48978C, UDI/DI 40195327325948 (each) 10195327325947 (case), Lot Numbers:  23LBP883;  12) REF DYNJ50428C, UDI/DI 40195327504039 (each) 10195327504038 (case), Lot Numbers:  23LBN301;  13) REF DYNJ53418B, UDI/DI 40195327372270 (each) 10195327372279 (case), Lot Numbers:  23LBO773;  14) REF DYNJ55479D, UDI/DI 40195327416769 (each) 10195327416768 (case), Lot Numbers:  23LBL444;  15) REF DYNJ58445A, UDI/DI 40195327585953 (each) 10195327585952 (case), Lot Numbers:  23LBU911;  16) REF DYNJ58566B, UDI/DI 40195327243228 (each) 10195327243227 (case), Lot Numbers:  23KBC919;  17) REF DYNJ59431, UDI/DI 40888277741257 (each) 10888277741256 (case), Lot Numbers:  24ABG210;  18) REF DYNJ60077A, UDI/DI 40193489862905 (each) 10193489862904 (case), Lot Numbers:  23LBO542;  19) REF DYNJ62111C, UDI/DI 40195327312146 (each) 10195327312145 (case), Lot Numbers:  23LBP204;  20) REF DYNJ65830A, UDI/DI 40195327588732 (each) 10195327588731 (case), Lot Numbers:  23LBR366;  21) REF DYNJ66821A, UDI/DI 40193489974929 (each) 10193489974928 (case), Lot Numbers:  23KBQ852;  22) REF DYNJ68883, UDI/DI 40193489848329 (each) 10193489848328 (case), Lot Numbers:  23KBC527;  23) REF DYNJ69729, UDI/DI 40193489973267 (each) 10193489973266 (case), Lot Numbers:  24ABD664;  24) REF DYNJ80004, UDI/DI 40195327005192 (each) 10195327005191 (case), Lot Numbers:  23LBP094;  25) REF DYNJ80763, UDI/DI 40195327076611 (each) 10195327076610 (case), Lot Numbers:  24ABG464;  26) REF DYNJ80763, UDI/DI 40195327076611 (each) 10195327076610 (case), Lot Numbers:  23LBU050;  27) REF DYNJ82626, UDI/DI 40195327199488 (each) 10195327199487 (case), Lot Numbers:  24ABN216;  28) REF DYNJ83155, UDI/DI 40195327236855 (each) 10195327236854 (case), Lot Numbers:  23LBV474;  29) REF DYNJ900583M, UDI/DI 40195327061853 (each) 10195327061852 (case), Lot Numbers:  24ABU214;  30) REF DYNJ905569B, UDI/DI 40193489995672 (each) 10193489995671 (case), Lot Numbers:  24ABJ966;  31) REF DYNJ907541A, UDI/DI 40195327054268 (each) 10195327054267 (case), Lot Numbers:  23KBT202;  32) REF LLSCASET01, UDI/DI 40080196120681 (each) 10080196120680 (case), Lot Numbers:  23LBM079;  33) REF SYNJ910011B, UDI/DI 40195327246809 (each) 10195327246808 (case), Lot Numbers:  24ABS212",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 9,
          "item": {
            "Field": "Distribution pattern",
            "Value": "Worldwide distribution - US Nationwide and the countries of Canada, Panama.",
            "Status": "recorded"
          }
        }
      ]
    }
  ]
}