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  "name": "Medtronic Arterial Cannulae packaged as:    a)\tDLP¿ Curved Metal Tip Arterial Cannula 20 Fr., Model Number 80020;   b)\tDLP¿ Curved Metal Tip Arterial Cannula 20 Fr., Model Number 80220;   c)\tDLP¿ Curved Metal Tip Arterial Cannula 20 Fr., Model Number 82020;   d)\tDLP¿ Curved Metal Tip Arterial Cannula 20 Fr., Model Number 87120;   e)\tDLP¿ Curved Metal Tip Arterial Cannula 22 Fr. , Model Number 80222;   f)\tDLP¿ Curved Metal Tip Arterial Cannula 22 Fr. , Model Number 87122;   g)\tDLP¿ Curved Tip Arterial Cannula 20 Fr., Model Number 87220;   h)\tDLP¿ Curved Tip Arterial Cannula 22 Fr., Model Number 87222;   i)\tDLP\" One-Piece Arterial Cannulae, Pediatric 6 Fr, Model Number 77006;   j)\tDLP\" One-Piece Pediatric Arterial Cannula 6 Fr, Model Number 77206;   k)\tDLP\" One-Piece Pediatric Arterial Cannula 8 Fr, Model Number 77008;   l)\tDLP\" One-Piece Pediatric Arterial Cannula 10 Fr, Model Number 77010;   m)\tDLP\" One-Piece Pediatric Arterial Cannula 10 Fr, Model Number 77110;   n)\tDLP\" One-Piece Pediatric Arterial Cannula 12 Fr, Model Number 77112;   o)\tEOPA\"   Elongated One Piece Arterial Cannula 20 Fr., Model Number 77420;   p)\tEOPA\"   Elongated One Piece Arterial Cannula 22 Fr., Model Number 77422;   q)\tEOPA\"   Elongated One Piece Arterial Cannula 22 Fr., Model Number 77522;   r)\tEOPA\"   Elongated One Piece Arterial Cannula 22 Fr., Model Number 77622;   s)\tEOPA\"   Elongated One Piece Arterial Cannula 24 Fr., Model Number 77524;   t)\tSelect Series\" Angled Tip Arterial Cannula 24Fr., Model Number 72424;   u)\tSelect Series\" Straight Tip Arterial Cannula 20 Fr., Model Number 72120;   v)\tSelect Series\" Straight Tip Arterial Cannula 24 Fr., Model Number 72224",
  "description": "FDA recall Z-1793-2024 — Medtronic Perfusion Systems is recalling Medtronic Arterial Cannulae packaged as:    a)\tDLP¿ Curved Metal Tip Arterial Cannula 20 Fr., Model Number 80020;   b)\tDLP¿ Curved Metal Tip Arterial Cannula 20 Fr., Model Number 80220;   c)\tDLP¿ Curved Metal Tip Arterial Cannula 20 Fr., Model Number 82020;   d)\tDLP¿ Curved Metal Tip Arterial Cannula 20 Fr., Model Number 87120;   e)\tDLP¿ Curved Metal Tip Arterial Cannula 22 Fr. , Model Number 80222;   f)\tDLP¿ Curved Metal Tip Arterial Cannula 22 Fr. , Model Number 87122;   g)\tDLP¿ Curved Tip Arterial Cannula 20 Fr., Model Number 87220;   h)\tDLP¿ Curved Tip Arterial Cannula 22 Fr., Model Number 87222;   i)\tDLP\" One-Piece Arterial Cannulae, Pediatric 6 Fr, Model Number 77006;   j)\tDLP\" One-Piece Pediatric Arterial Cannula 6 Fr, Model Number 77206;   k)\tDLP\" One-Piece Pediatric Arterial Cannula 8 Fr, Model Number 77008;   l)\tDLP\" One-Piece Pediatric Arterial Cannula 10 Fr, Model Number 77010;   m)\tDLP\" One-Piece Pediatric Arterial Cannula 10 Fr, Model Number 77110;   n)\tDLP\" One-Piece Pediatric Arterial Cannula 12 Fr, Model Number 77112;   o)\tEOPA\"   Elongated One Piece Arterial Cannula 20 Fr., Model Number 77420;   p)\tEOPA\"   Elongated One Piece Arterial Cannula 22 Fr., Model Number 77422;   q)\tEOPA\"   Elongated One Piece Arterial Cannula 22 Fr., Model Number 77522;   r)\tEOPA\"   Elongated One Piece Arterial Cannula 22 Fr., Model Number 77622;   s)\tEOPA\"   Elongated One Piece Arterial Cannula 24 Fr., Model Number 77524;   t)\tSelect Series\" Angled Tip Arterial Cannula 24Fr., Model Number 72424;   u)\tSelect Series\" Straight Tip Arterial Cannula 20 Fr., Model Number 72120;   v)\tSelect Series\" Straight Tip Arterial Cannula 24 Fr., Model Number 72224 (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": "openFDA drug & device enforcement (recall) reports",
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    "creator": {
      "@type": "schema:GovernmentOrganization",
      "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-1793-2024&lang=eng",
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    "@type": "schema:MedicalDevice",
    "name": "Medtronic Arterial Cannulae packaged as:    a)\tDLP¿ Curved Metal Tip Arterial Cannula 20 Fr., Model Number 80020;   b)\tDLP¿ Curved Metal Tip Arterial Cannula 20 Fr., Model Number 80220;   c)\tDLP¿ Curved Metal Tip Arterial Cannula 20 Fr., Model Number 82020;   d)\tDLP¿ Curved Metal Tip Arterial Cannula 20 Fr., Model Number 87120;   e)\tDLP¿ Curved Metal Tip Arterial Cannula 22 Fr. , Model Number 80222;   f)\tDLP¿ Curved Metal Tip Arterial Cannula 22 Fr. , Model Number 87122;   g)\tDLP¿ Curved Tip Arterial Cannula 20 Fr., Model Number 87220;   h)\tDLP¿ Curved Tip Arterial Cannula 22 Fr., Model Number 87222;   i)\tDLP\" One-Piece Arterial Cannulae, Pediatric 6 Fr, Model Number 77006;   j)\tDLP\" One-Piece Pediatric Arterial Cannula 6 Fr, Model Number 77206;   k)\tDLP\" One-Piece Pediatric Arterial Cannula 8 Fr, Model Number 77008;   l)\tDLP\" One-Piece Pediatric Arterial Cannula 10 Fr, Model Number 77010;   m)\tDLP\" One-Piece Pediatric Arterial Cannula 10 Fr, Model Number 77110;   n)\tDLP\" One-Piece Pediatric Arterial Cannula 12 Fr, Model Number 77112;   o)\tEOPA\"   Elongated One Piece Arterial Cannula 20 Fr., Model Number 77420;   p)\tEOPA\"   Elongated One Piece Arterial Cannula 22 Fr., Model Number 77422;   q)\tEOPA\"   Elongated One Piece Arterial Cannula 22 Fr., Model Number 77522;   r)\tEOPA\"   Elongated One Piece Arterial Cannula 22 Fr., Model Number 77622;   s)\tEOPA\"   Elongated One Piece Arterial Cannula 24 Fr., Model Number 77524;   t)\tSelect Series\" Angled Tip Arterial Cannula 24Fr., Model Number 72424;   u)\tSelect Series\" Straight Tip Arterial Cannula 20 Fr., Model Number 72120;   v)\tSelect Series\" Straight Tip Arterial Cannula 24 Fr., Model Number 72224",
    "manufacturer": {
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      "name": "Medtronic Perfusion Systems"
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  "claims": [
    {
      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-1793-2024/enforcement-record",
      "@type": "schema:Claim",
      "name": "FDA recall Z-1793-2024: Medtronic Perfusion Systems is recalling Medtronic Arterial Cannulae packaged as:    a)\tDLP¿ Curved Metal Tip Arterial Cannula 20 Fr., Model Number 80020;   b)\tDLP¿ Curved Metal Tip Arterial Cannula 20 Fr., Model Number 80220;   c)\tDLP¿ Curved Metal Tip Arterial Cannula 20 Fr., Model Number 82020;   d)\tDLP¿ Curved Metal Tip Arterial Cannula 20 Fr., Model Number 87120;   e)\tDLP¿ Curved Metal Tip Arterial Cannula 22 Fr. , Model Number 80222;   f)\tDLP¿ Curved Metal Tip Arterial Cannula 22 Fr. , Model Number 87122;   g)\tDLP¿ Curved Tip Arterial Cannula 20 Fr., Model Number 87220;   h)\tDLP¿ Curved Tip Arterial Cannula 22 Fr., Model Number 87222;   i)\tDLP\" One-Piece Arterial Cannulae, Pediatric 6 Fr, Model Number 77006;   j)\tDLP\" One-Piece Pediatric Arterial Cannula 6 Fr, Model Number 77206;   k)\tDLP\" One-Piece Pediatric Arterial Cannula 8 Fr, Model Number 77008;   l)\tDLP\" One-Piece Pediatric Arterial Cannula 10 Fr, Model Number 77010;   m)\tDLP\" One-Piece Pediatric Arterial Cannula 10 Fr, Model Number 77110;   n)\tDLP\" One-Piece Pediatric Arterial Cannula 12 Fr, Model Number 77112;   o)\tEOPA\"   Elongated One Piece Arterial Cannula 20 Fr., Model Number 77420;   p)\tEOPA\"   Elongated One Piece Arterial Cannula 22 Fr., Model Number 77422;   q)\tEOPA\"   Elongated One Piece Arterial Cannula 22 Fr., Model Number 77522;   r)\tEOPA\"   Elongated One Piece Arterial Cannula 22 Fr., Model Number 77622;   s)\tEOPA\"   Elongated One Piece Arterial Cannula 24 Fr., Model Number 77524;   t)\tSelect Series\" Angled Tip Arterial Cannula 24Fr., Model Number 72424;   u)\tSelect Series\" Straight Tip Arterial Cannula 20 Fr., Model Number 72120;   v)\tSelect Series\" Straight Tip Arterial Cannula 24 Fr., Model Number 72224",
      "text": "The FDA logged enforcement record Z-1793-2024: Medtronic Perfusion Systems is voluntarily recalling Medtronic Arterial Cannulae packaged as:    a)\tDLP¿ Curved Metal Tip Arterial Cannula 20 Fr., Model Number 80020;   b)\tDLP¿ Curved Metal Tip Arterial Cannula 20 Fr., Model Number 80220;   c)\tDLP¿ Curved Metal Tip Arterial Cannula 20 Fr., Model Number 82020;   d)\tDLP¿ Curved Metal Tip Arterial Cannula 20 Fr., Model Number 87120;   e)\tDLP¿ Curved Metal Tip Arterial Cannula 22 Fr. , Model Number 80222;   f)\tDLP¿ Curved Metal Tip Arterial Cannula 22 Fr. , Model Number 87122;   g)\tDLP¿ Curved Tip Arterial Cannula 20 Fr., Model Number 87220;   h)\tDLP¿ Curved Tip Arterial Cannula 22 Fr., Model Number 87222;   i)\tDLP\" One-Piece Arterial Cannulae, Pediatric 6 Fr, Model Number 77006;   j)\tDLP\" One-Piece Pediatric Arterial Cannula 6 Fr, Model Number 77206;   k)\tDLP\" One-Piece Pediatric Arterial Cannula 8 Fr, Model Number 77008;   l)\tDLP\" One-Piece Pediatric Arterial Cannula 10 Fr, Model Number 77010;   m)\tDLP\" One-Piece Pediatric Arterial Cannula 10 Fr, Model Number 77110;   n)\tDLP\" One-Piece Pediatric Arterial Cannula 12 Fr, Model Number 77112;   o)\tEOPA\"   Elongated One Piece Arterial Cannula 20 Fr., Model Number 77420;   p)\tEOPA\"   Elongated One Piece Arterial Cannula 22 Fr., Model Number 77422;   q)\tEOPA\"   Elongated One Piece Arterial Cannula 22 Fr., Model Number 77522;   r)\tEOPA\"   Elongated One Piece Arterial Cannula 22 Fr., Model Number 77622;   s)\tEOPA\"   Elongated One Piece Arterial Cannula 24 Fr., Model Number 77524;   t)\tSelect Series\" Angled Tip Arterial Cannula 24Fr., Model Number 72424;   u)\tSelect Series\" Straight Tip Arterial Cannula 20 Fr., Model Number 72120;   v)\tSelect Series\" Straight Tip Arterial Cannula 24 Fr., Model Number 72224 — reason: Potential for unsealed sterile packing.. Status: Ongoing — the recall is still being carried out.. Initiated 2024-03-19. Affected lots/codes: a) Model Number 80020, GTIN 20643169485703, Lot Numbers:  2023040597, 2023041061, 202305C247;   b) Model Number 80220, GTIN 20643169485734, Lot Numbers:  2023031390, 2023040098, 202305C249, 202310C155;   c) Model Number 82020, GTIN 20643169485536, Lot Numbers:  2023041063, 2023041396, 202305C253;   d) Model Number 87120, GTIN 00673978187105, Lot Numbers:  2023040600;  GTIN 20613994879114, Lot Numbers:  2023040600, 2023041066, 202306C018;   e) Model Number 80222, GTIN 20643169485741, Lot Numbers:  2023041062, 202308C058;   f) Model Number 87122, GTIN 00613994879103, Lot Numbers:  2023040601; GTIN 20613994879107, Lot Numbers:  2023040601, 2023041067, 202306C017;   g) Model Number 87220, GTIN 00643169485563, Lot Numbers:  2023031282, 2023040602, 2023041068; GTIN 20643169485567, Lot Numbers:  2023031282, 2023031283, 2023031391, 2023040602, 2023041068, 202306C006, 202306C247;   h) Model Number 87222, GTIN 00643169485570, Lot Numbers:  2023041408; GTIN 20643169485574, Lot Numbers:  2023041069, 2023041408, 202306C007;   i) Model Number 77006, GTIN 20763000091013, Lot Numbers:  2023040943, 202306C056;   j) Model Number 77206, GTIN 20763000091020, Lot Numbers:  2023041347, 202308C108;   k) Model Number 77008, GTIN 20763000091105, Lot Numbers:  2023040944, 2023040946, 02306C020, 202308C084;   l) Model Number 77010, GTIN 20763000091112, Lot Numbers:  2023041337, 202306C023;   m) Model Number 77110, GTIN 00673978185989, Lot Numbers:  2023041342; GTIN 20763000091174, Lot Numbers:  2023041342, 202308C104;    n) Model Number 77112, GTIN 00673978186009, Lot Numbers:  2023041343; GTIN 20763000091181, Lot Numbers:  2023041343, 202308C106;   o) Model Number 77420, GTIN 20763000135625, Lot Numbers:  2023040668, 2023040671, 202306C032, 202307C005;   p) Model Number 77422, GTIN 20763000135632, Lot Numbers:  2023040966, 2023041355, 202306C043, 202306C046;   q) Model Number 77522, GTIN 20763000135557, Lot Numbers:  2023041361, 2023041364, 202306C051;   r) Model Number 77622, GTIN 00763000135676, Lot Numbers:  2023040971; GTIN 20763000135670, Lot Numbers:  2023040971, 2023040974, 2023040978, 2023040980, 202306C061, 202307C029, 202307C030;    s) Model Number 77524, GTIN 20763000135564, Lot Numbers:  2023041365, 202306C052;  t) Model Number 72424, GTIN 20643169485468, Lot Numbers:  2023040940;   u) Model Number 72120, GTIN 00643169485938, Lot Numbers:  2023041326; GTIN 20643169485932, lot Numbers:  2023041326, 202305C184;   v) Model Number 72224, GTIN 20613994879701, Lot Numbers:  2023041332. A RECORDED FDA enforcement action (occurred=true).",
      "claimType": "official_fact",
      "reviewStatus": "current",
      "commercialInfluence": false,
      "epistemicStatus": {
        "occurred": true,
        "supported": true,
        "adjudged": true,
        "operative": true
      },
      "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-1793-2024&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-1793-2024&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-1793-2024/fda-classification",
      "@type": "schema:Claim",
      "name": "FDA classified recall Z-1793-2024 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-1793-2024&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-1793-2024&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-1793-2024/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."
    }
  ],
  "hasPart": [
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      "@type": "schema:ItemList",
      "name": "FDA recall details — Z-1793-2024",
      "numberOfItems": 9,
      "itemListElement": [
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          "@type": "schema:ListItem",
          "position": 1,
          "item": {
            "Field": "Recall number",
            "Value": "Z-1793-2024",
            "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": "Medtronic Perfusion Systems",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 6,
          "item": {
            "Field": "Reason",
            "Value": "Potential for unsealed sterile packing.",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 7,
          "item": {
            "Field": "Initiated",
            "Value": "2024-03-19",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 8,
          "item": {
            "Field": "Lot/code info",
            "Value": "a) Model Number 80020, GTIN 20643169485703, Lot Numbers:  2023040597, 2023041061, 202305C247;   b) Model Number 80220, GTIN 20643169485734, Lot Numbers:  2023031390, 2023040098, 202305C249, 202310C155;   c) Model Number 82020, GTIN 20643169485536, Lot Numbers:  2023041063, 2023041396, 202305C253;   d) Model Number 87120, GTIN 00673978187105, Lot Numbers:  2023040600;  GTIN 20613994879114, Lot Numbers:  2023040600, 2023041066, 202306C018;   e) Model Number 80222, GTIN 20643169485741, Lot Numbers:  2023041062, 202308C058;   f) Model Number 87122, GTIN 00613994879103, Lot Numbers:  2023040601; GTIN 20613994879107, Lot Numbers:  2023040601, 2023041067, 202306C017;   g) Model Number 87220, GTIN 00643169485563, Lot Numbers:  2023031282, 2023040602, 2023041068; GTIN 20643169485567, Lot Numbers:  2023031282, 2023031283, 2023031391, 2023040602, 2023041068, 202306C006, 202306C247;   h) Model Number 87222, GTIN 00643169485570, Lot Numbers:  2023041408; GTIN 20643169485574, Lot Numbers:  2023041069, 2023041408, 202306C007;   i) Model Number 77006, GTIN 20763000091013, Lot Numbers:  2023040943, 202306C056;   j) Model Number 77206, GTIN 20763000091020, Lot Numbers:  2023041347, 202308C108;   k) Model Number 77008, GTIN 20763000091105, Lot Numbers:  2023040944, 2023040946, 02306C020, 202308C084;   l) Model Number 77010, GTIN 20763000091112, Lot Numbers:  2023041337, 202306C023;   m) Model Number 77110, GTIN 00673978185989, Lot Numbers:  2023041342; GTIN 20763000091174, Lot Numbers:  2023041342, 202308C104;    n) Model Number 77112, GTIN 00673978186009, Lot Numbers:  2023041343; GTIN 20763000091181, Lot Numbers:  2023041343, 202308C106;   o) Model Number 77420, GTIN 20763000135625, Lot Numbers:  2023040668, 2023040671, 202306C032, 202307C005;   p) Model Number 77422, GTIN 20763000135632, Lot Numbers:  2023040966, 2023041355, 202306C043, 202306C046;   q) Model Number 77522, GTIN 20763000135557, Lot Numbers:  2023041361, 2023041364, 202306C051;   r) Model Number 77622, GTIN 00763000135676, Lot Numbers:  2023040971; GTIN 20763000135670, Lot Numbers:  2023040971, 2023040974, 2023040978, 2023040980, 202306C061, 202307C029, 202307C030;    s) Model Number 77524, GTIN 20763000135564, Lot Numbers:  2023041365, 202306C052;  t) Model Number 72424, GTIN 20643169485468, Lot Numbers:  2023040940;   u) Model Number 72120, GTIN 00643169485938, Lot Numbers:  2023041326; GTIN 20643169485932, lot Numbers:  2023041326, 202305C184;   v) Model Number 72224, GTIN 20613994879701, Lot Numbers:  2023041332",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 9,
          "item": {
            "Field": "Distribution pattern",
            "Value": "Worldwide distribution.",
            "Status": "recorded"
          }
        }
      ]
    }
  ]
}