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  "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-3152-2024.jsonld",
  "@type": "schema:Dataset",
  "name": "2090 Programmers with serial number prefixes PKK0 and PKK1:    a)\t2090, Product Description:  PRGM 2090  PROGRAMMER-PORTABLE CRM;   b)\t209031, Product Description:  PROGRAMMER 209031 PORTABLE CRM;   c)\t2090AA, Product Description:  PROGRAMMER 2090AA PORTABLE CRM;   d)\t2090AA4, Product Description:  2090AA4  PROGRAMMER-PORTABLE CRM;   e)\t2090AC, Product Description:  SFTWR 2090AC  PROGRAMMER-PORTABLE CRM W/;   f)\t2090AM, Product Description:  PROGRAMMER CARELINK HONG KONG ASIA;   g)\t2090CHEN, Product Description:  PRGM 2090CHEN  PKG-ASSY PROGRAMMER 2090;   h)\t2090CHFR, Product Description:  PRGM 2090CHFR  PKG-ASSY PROGRAMMER 2090;   i)\t2090CL, Product Description:  PROGRAMMER 2090CL INTL-JAPAN MKT;   j)\t2090EN, Product Description:  PRGM 2090EN  PKG-ASSY PROGRAMMER 2090 UK;   k)\t2090FR, Product Description:  PRGM 2090FR  PKG-ASSY PROGRAMMER 2090 IN;   l)\t2090LDEN, Product Description:  PRGM 2090LDEN  PROGRAMMER-PORTABLE LOANE;   m)\t2090NL, Product Description:  PRGM 2090NL  PKG-ASSY PROGRAMMER 2090 IN;   n)\t2090W, Product Description:  PROGRAMMER  2090W TELEMETRY C;   o)\t2090WCHDE, Product Description:  PROGRAMMER 2090WCHDE SWISS-GERMAN;   p)\t2090WCHEN, Product Description:  PROGRAMMER 2090WCHEN SWISS-ENGLISH;   q)\t2090WCHFR, Product Description:  PROGRAMMER 2090WCHFR SWISS-FRENCH;   r)\t2090WDE, Product Description:  PROGRAMMER 2090WDE GERMAN MKT;   s)\t2090WFR, Product Description:  PROGRAMMER 2090WFR FRENCH MKT;   t)\t2090WLD, Product Description:  PROG 2090WLD ALL LANGUAGES W/ANALYZER;   u)\t2090WNL, Product Description:  PROGRAMMER 2090WNL NETHERLANDS MKT",
  "description": "FDA recall Z-3152-2024 — Medtronic Inc. is recalling 2090 Programmers with serial number prefixes PKK0 and PKK1:    a)\t2090, Product Description:  PRGM 2090  PROGRAMMER-PORTABLE CRM;   b)\t209031, Product Description:  PROGRAMMER 209031 PORTABLE CRM;   c)\t2090AA, Product Description:  PROGRAMMER 2090AA PORTABLE CRM;   d)\t2090AA4, Product Description:  2090AA4  PROGRAMMER-PORTABLE CRM;   e)\t2090AC, Product Description:  SFTWR 2090AC  PROGRAMMER-PORTABLE CRM W/;   f)\t2090AM, Product Description:  PROGRAMMER CARELINK HONG KONG ASIA;   g)\t2090CHEN, Product Description:  PRGM 2090CHEN  PKG-ASSY PROGRAMMER 2090;   h)\t2090CHFR, Product Description:  PRGM 2090CHFR  PKG-ASSY PROGRAMMER 2090;   i)\t2090CL, Product Description:  PROGRAMMER 2090CL INTL-JAPAN MKT;   j)\t2090EN, Product Description:  PRGM 2090EN  PKG-ASSY PROGRAMMER 2090 UK;   k)\t2090FR, Product Description:  PRGM 2090FR  PKG-ASSY PROGRAMMER 2090 IN;   l)\t2090LDEN, Product Description:  PRGM 2090LDEN  PROGRAMMER-PORTABLE LOANE;   m)\t2090NL, Product Description:  PRGM 2090NL  PKG-ASSY PROGRAMMER 2090 IN;   n)\t2090W, Product Description:  PROGRAMMER  2090W TELEMETRY C;   o)\t2090WCHDE, Product Description:  PROGRAMMER 2090WCHDE SWISS-GERMAN;   p)\t2090WCHEN, Product Description:  PROGRAMMER 2090WCHEN SWISS-ENGLISH;   q)\t2090WCHFR, Product Description:  PROGRAMMER 2090WCHFR SWISS-FRENCH;   r)\t2090WDE, Product Description:  PROGRAMMER 2090WDE GERMAN MKT;   s)\t2090WFR, Product Description:  PROGRAMMER 2090WFR FRENCH MKT;   t)\t2090WLD, Product Description:  PROG 2090WLD ALL LANGUAGES W/ANALYZER;   u)\t2090WNL, Product Description:  PROGRAMMER 2090WNL NETHERLANDS MKT (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/",
  "isAccessibleForFree": true,
  "isPartOf": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/",
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  "seeAlso": "https://agenticu.ryanjhunter.workers.dev/commons/the-research-object",
  "dateModified": "2026-06-24T07:02:03.626072+00:00",
  "isBasedOn": {
    "@type": "schema:Dataset",
    "name": "openFDA drug & device enforcement (recall) reports",
    "url": "https://open.fda.gov/apis/drug/enforcement/",
    "creator": {
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      "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-3152-2024&lang=eng",
  "about": {
    "@type": "schema:MedicalDevice",
    "name": "2090 Programmers with serial number prefixes PKK0 and PKK1:    a)\t2090, Product Description:  PRGM 2090  PROGRAMMER-PORTABLE CRM;   b)\t209031, Product Description:  PROGRAMMER 209031 PORTABLE CRM;   c)\t2090AA, Product Description:  PROGRAMMER 2090AA PORTABLE CRM;   d)\t2090AA4, Product Description:  2090AA4  PROGRAMMER-PORTABLE CRM;   e)\t2090AC, Product Description:  SFTWR 2090AC  PROGRAMMER-PORTABLE CRM W/;   f)\t2090AM, Product Description:  PROGRAMMER CARELINK HONG KONG ASIA;   g)\t2090CHEN, Product Description:  PRGM 2090CHEN  PKG-ASSY PROGRAMMER 2090;   h)\t2090CHFR, Product Description:  PRGM 2090CHFR  PKG-ASSY PROGRAMMER 2090;   i)\t2090CL, Product Description:  PROGRAMMER 2090CL INTL-JAPAN MKT;   j)\t2090EN, Product Description:  PRGM 2090EN  PKG-ASSY PROGRAMMER 2090 UK;   k)\t2090FR, Product Description:  PRGM 2090FR  PKG-ASSY PROGRAMMER 2090 IN;   l)\t2090LDEN, Product Description:  PRGM 2090LDEN  PROGRAMMER-PORTABLE LOANE;   m)\t2090NL, Product Description:  PRGM 2090NL  PKG-ASSY PROGRAMMER 2090 IN;   n)\t2090W, Product Description:  PROGRAMMER  2090W TELEMETRY C;   o)\t2090WCHDE, Product Description:  PROGRAMMER 2090WCHDE SWISS-GERMAN;   p)\t2090WCHEN, Product Description:  PROGRAMMER 2090WCHEN SWISS-ENGLISH;   q)\t2090WCHFR, Product Description:  PROGRAMMER 2090WCHFR SWISS-FRENCH;   r)\t2090WDE, Product Description:  PROGRAMMER 2090WDE GERMAN MKT;   s)\t2090WFR, Product Description:  PROGRAMMER 2090WFR FRENCH MKT;   t)\t2090WLD, Product Description:  PROG 2090WLD ALL LANGUAGES W/ANALYZER;   u)\t2090WNL, Product Description:  PROGRAMMER 2090WNL NETHERLANDS MKT",
    "manufacturer": {
      "@type": "schema:Organization",
      "name": "Medtronic Inc."
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  },
  "claims": [
    {
      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-3152-2024/enforcement-record",
      "@type": "schema:Claim",
      "name": "FDA recall Z-3152-2024: Medtronic Inc. is recalling 2090 Programmers with serial number prefixes PKK0 and PKK1:    a)\t2090, Product Description:  PRGM 2090  PROGRAMMER-PORTABLE CRM;   b)\t209031, Product Description:  PROGRAMMER 209031 PORTABLE CRM;   c)\t2090AA, Product Description:  PROGRAMMER 2090AA PORTABLE CRM;   d)\t2090AA4, Product Description:  2090AA4  PROGRAMMER-PORTABLE CRM;   e)\t2090AC, Product Description:  SFTWR 2090AC  PROGRAMMER-PORTABLE CRM W/;   f)\t2090AM, Product Description:  PROGRAMMER CARELINK HONG KONG ASIA;   g)\t2090CHEN, Product Description:  PRGM 2090CHEN  PKG-ASSY PROGRAMMER 2090;   h)\t2090CHFR, Product Description:  PRGM 2090CHFR  PKG-ASSY PROGRAMMER 2090;   i)\t2090CL, Product Description:  PROGRAMMER 2090CL INTL-JAPAN MKT;   j)\t2090EN, Product Description:  PRGM 2090EN  PKG-ASSY PROGRAMMER 2090 UK;   k)\t2090FR, Product Description:  PRGM 2090FR  PKG-ASSY PROGRAMMER 2090 IN;   l)\t2090LDEN, Product Description:  PRGM 2090LDEN  PROGRAMMER-PORTABLE LOANE;   m)\t2090NL, Product Description:  PRGM 2090NL  PKG-ASSY PROGRAMMER 2090 IN;   n)\t2090W, Product Description:  PROGRAMMER  2090W TELEMETRY C;   o)\t2090WCHDE, Product Description:  PROGRAMMER 2090WCHDE SWISS-GERMAN;   p)\t2090WCHEN, Product Description:  PROGRAMMER 2090WCHEN SWISS-ENGLISH;   q)\t2090WCHFR, Product Description:  PROGRAMMER 2090WCHFR SWISS-FRENCH;   r)\t2090WDE, Product Description:  PROGRAMMER 2090WDE GERMAN MKT;   s)\t2090WFR, Product Description:  PROGRAMMER 2090WFR FRENCH MKT;   t)\t2090WLD, Product Description:  PROG 2090WLD ALL LANGUAGES W/ANALYZER;   u)\t2090WNL, Product Description:  PROGRAMMER 2090WNL NETHERLANDS MKT",
      "text": "The FDA logged enforcement record Z-3152-2024: Medtronic Inc. is voluntarily recalling 2090 Programmers with serial number prefixes PKK0 and PKK1:    a)\t2090, Product Description:  PRGM 2090  PROGRAMMER-PORTABLE CRM;   b)\t209031, Product Description:  PROGRAMMER 209031 PORTABLE CRM;   c)\t2090AA, Product Description:  PROGRAMMER 2090AA PORTABLE CRM;   d)\t2090AA4, Product Description:  2090AA4  PROGRAMMER-PORTABLE CRM;   e)\t2090AC, Product Description:  SFTWR 2090AC  PROGRAMMER-PORTABLE CRM W/;   f)\t2090AM, Product Description:  PROGRAMMER CARELINK HONG KONG ASIA;   g)\t2090CHEN, Product Description:  PRGM 2090CHEN  PKG-ASSY PROGRAMMER 2090;   h)\t2090CHFR, Product Description:  PRGM 2090CHFR  PKG-ASSY PROGRAMMER 2090;   i)\t2090CL, Product Description:  PROGRAMMER 2090CL INTL-JAPAN MKT;   j)\t2090EN, Product Description:  PRGM 2090EN  PKG-ASSY PROGRAMMER 2090 UK;   k)\t2090FR, Product Description:  PRGM 2090FR  PKG-ASSY PROGRAMMER 2090 IN;   l)\t2090LDEN, Product Description:  PRGM 2090LDEN  PROGRAMMER-PORTABLE LOANE;   m)\t2090NL, Product Description:  PRGM 2090NL  PKG-ASSY PROGRAMMER 2090 IN;   n)\t2090W, Product Description:  PROGRAMMER  2090W TELEMETRY C;   o)\t2090WCHDE, Product Description:  PROGRAMMER 2090WCHDE SWISS-GERMAN;   p)\t2090WCHEN, Product Description:  PROGRAMMER 2090WCHEN SWISS-ENGLISH;   q)\t2090WCHFR, Product Description:  PROGRAMMER 2090WCHFR SWISS-FRENCH;   r)\t2090WDE, Product Description:  PROGRAMMER 2090WDE GERMAN MKT;   s)\t2090WFR, Product Description:  PROGRAMMER 2090WFR FRENCH MKT;   t)\t2090WLD, Product Description:  PROG 2090WLD ALL LANGUAGES W/ANALYZER;   u)\t2090WNL, Product Description:  PROGRAMMER 2090WNL NETHERLANDS MKT — reason: Medtronic CareLink 2090 programmers with serial number prefixes PKK0 and PKK1 have the potential for autonomous cursor motion when Finger Touchscreen capability is enabled by software version 3.2 or higher.. Status: Ongoing — the recall is still being carried out.. Initiated 2024-07-11. Affected lots/codes: 2090 Programmers with serial number prefixes PKK0 and PKK1:   a) GTIN: 00613994136480, 00613994136497, 00613994136503, 00613994136510, 00613994136527, 00613994136534, 00613994136565, 00613994136596, 00613994136619, 00613994136626, 00613994175076, 00613994175083, 00613994175090, 00613994175106, 00613994175120, 00613994175137, 00613994175144, 00613994175151, 00613994175168, 00613994175175, 00613994175182, 00613994175205, 00613994175212, 00613994175229, 00613994175236, 00613994175243, 00613994175250, 00613994175267, 00613994175281, 00613994175298, 00613994175304, 00613994175311, 00613994175328, 00613994175335, 00613994175342, 00613994175366, 00613994175373, 00613994175380, 00613994175397, 00613994175403, 00613994175410, 00613994175434, 00613994175465, 00613994175489, 00613994175540, 00613994175588, 00613994175595, 00613994203182, 00613994360922, 00613994434883, 00613994434890, 00613994434944, 00613994435002, 00613994435255, 00613994435316, 00613994580863, 00613994580894, 00613994580931, 00613994580962, 00613994581013, 00613994581051, 00613994581075, 00613994581105, 00613994581150, 00613994581167, 00613994581174, 00613994581181, 00613994581204, 00613994581211, 00613994581228, 00613994581235, 00613994581242, 00613994581549, 00613994581570, 00613994581587, 00613994581594, 00613994581624, 00643169440128, 00643169440166, 00643169440173, 00643169440197, 00643169440203, 00643169440937, 00643169537750, 00643169537774, 00643169537811, 00643169537828, 00643169537835, 00643169537842, 00643169537859, 00643169537866, 00643169537880, 00643169537910, 00643169537927, 00643169538016, 00643169629004, 00643169629011, 00643169629028, 00643169629035, 00643169629042, 00643169629066, 00721902246227, 00721902246234, 00721902246241, 00721902246265, 00721902246289, 00721902246302, 00721902246326, 00721902246333;   b) GTIN:  00721902171222;  c)  GTIN:  00721902171079;  d)  GTIN:  00721902824692;  e)  GTIN:  00721902059100;  f)  GTIN:  00721902171154;  g)  GTIN:  00721902246357;  h)  GTIN:  00721902246364;  i)  GTIN:  00721902480201;  j)  GTIN:  00721902246159, 00721902246173;  k)  GTIN:  00721902246203;  l)  GTIN:  00721902841903;  m)  GTIN:  00721902246272;  n)  GTIN:  00613994127631, 00613994435354, 00613994581549, 00885074301440, 00885074310596, 00885074310633, 00885074310657, 00885074310930, 00885074312866, 00885074312873, 00885074313047, 00885074313108, 00885074313115, 00885074313139, 00885074313146, 00885074313153, 00885074313160;   o)  GTIN:  00885074313191;  p)  GTIN:  00885074313177;  q) GTIN:  00885074313184;  r)  GTIN:  00885074314921;  s)  GTIN:  00885074313009;  t)  GTIN:  00885074357416;  u)  GTIN:  00885074313122. 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-3152-2024&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-3152-2024&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-3152-2024/fda-classification",
      "@type": "schema:Claim",
      "name": "FDA classified recall Z-3152-2024 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
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      "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-3152-2024&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-3152-2024&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-3152-2024/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": {
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        "supported": true,
        "adjudged": false,
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      },
      "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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      "name": "FDA recall details — Z-3152-2024",
      "numberOfItems": 9,
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          "position": 1,
          "item": {
            "Field": "Recall number",
            "Value": "Z-3152-2024",
            "Status": "recorded"
          }
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          "position": 2,
          "item": {
            "Field": "Product type",
            "Value": "Devices",
            "Status": "recorded"
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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"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 5,
          "item": {
            "Field": "Recalling firm",
            "Value": "Medtronic Inc.",
            "Status": "recorded"
          }
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          "position": 6,
          "item": {
            "Field": "Reason",
            "Value": "Medtronic CareLink 2090 programmers with serial number prefixes PKK0 and PKK1 have the potential for autonomous cursor motion when Finger Touchscreen capability is enabled by software version 3.2 or higher.",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 7,
          "item": {
            "Field": "Initiated",
            "Value": "2024-07-11",
            "Status": "recorded"
          }
        },
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          "position": 8,
          "item": {
            "Field": "Lot/code info",
            "Value": "2090 Programmers with serial number prefixes PKK0 and PKK1:   a) GTIN: 00613994136480, 00613994136497, 00613994136503, 00613994136510, 00613994136527, 00613994136534, 00613994136565, 00613994136596, 00613994136619, 00613994136626, 00613994175076, 00613994175083, 00613994175090, 00613994175106, 00613994175120, 00613994175137, 00613994175144, 00613994175151, 00613994175168, 00613994175175, 00613994175182, 00613994175205, 00613994175212, 00613994175229, 00613994175236, 00613994175243, 00613994175250, 00613994175267, 00613994175281, 00613994175298, 00613994175304, 00613994175311, 00613994175328, 00613994175335, 00613994175342, 00613994175366, 00613994175373, 00613994175380, 00613994175397, 00613994175403, 00613994175410, 00613994175434, 00613994175465, 00613994175489, 00613994175540, 00613994175588, 00613994175595, 00613994203182, 00613994360922, 00613994434883, 00613994434890, 00613994434944, 00613994435002, 00613994435255, 00613994435316, 00613994580863, 00613994580894, 00613994580931, 00613994580962, 00613994581013, 00613994581051, 00613994581075, 00613994581105, 00613994581150, 00613994581167, 00613994581174, 00613994581181, 00613994581204, 00613994581211, 00613994581228, 00613994581235, 00613994581242, 00613994581549, 00613994581570, 00613994581587, 00613994581594, 00613994581624, 00643169440128, 00643169440166, 00643169440173, 00643169440197, 00643169440203, 00643169440937, 00643169537750, 00643169537774, 00643169537811, 00643169537828, 00643169537835, 00643169537842, 00643169537859, 00643169537866, 00643169537880, 00643169537910, 00643169537927, 00643169538016, 00643169629004, 00643169629011, 00643169629028, 00643169629035, 00643169629042, 00643169629066, 00721902246227, 00721902246234, 00721902246241, 00721902246265, 00721902246289, 00721902246302, 00721902246326, 00721902246333;   b) GTIN:  00721902171222;  c)  GTIN:  00721902171079;  d)  GTIN:  00721902824692;  e)  GTIN:  00721902059100;  f)  GTIN:  00721902171154;  g)  GTIN:  00721902246357;  h)  GTIN:  00721902246364;  i)  GTIN:  00721902480201;  j)  GTIN:  00721902246159, 00721902246173;  k)  GTIN:  00721902246203;  l)  GTIN:  00721902841903;  m)  GTIN:  00721902246272;  n)  GTIN:  00613994127631, 00613994435354, 00613994581549, 00885074301440, 00885074310596, 00885074310633, 00885074310657, 00885074310930, 00885074312866, 00885074312873, 00885074313047, 00885074313108, 00885074313115, 00885074313139, 00885074313146, 00885074313153, 00885074313160;   o)  GTIN:  00885074313191;  p)  GTIN:  00885074313177;  q) GTIN:  00885074313184;  r)  GTIN:  00885074314921;  s)  GTIN:  00885074313009;  t)  GTIN:  00885074357416;  u)  GTIN:  00885074313122",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 9,
          "item": {
            "Field": "Distribution pattern",
            "Value": "Worldwide distribution.",
            "Status": "recorded"
          }
        }
      ]
    }
  ]
}