{
  "@context": {
    "schema": "https://schema.org/",
    "au": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/vocab/agent-native#",
    "@vocab": "https://schema.org/",
    "claims": {
      "@id": "au:claims",
      "@container": "@list"
    },
    "epistemicStatus": "au:epistemicStatus",
    "occurred": "au:occurred",
    "supported": "au:supported",
    "adjudged": "au:adjudged",
    "operative": "au:operative",
    "grounding": "au:grounding",
    "groundingType": "au:groundingType",
    "adjudicator": "au:adjudicator",
    "source": "au:source",
    "sourceUrl": "au:sourceUrl",
    "value": "au:value",
    "claimType": "au:claimType",
    "reviewStatus": "au:reviewStatus",
    "commercialInfluence": "au:commercialInfluence",
    "falsifier": "au:falsifier"
  },
  "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-0825-2024.jsonld",
  "@type": "schema:Dataset",
  "name": "Custom procedural convenience kits and trays, general & plastic surgery, labeled as:    a)\tBRACHY THERAPY PROCEDURE PAC, kit number AGBR90E;   b)\tBRACHY THERAPY PROCEDURE PAC, kit number AGBR90E;   c)\tMINI MINOR AGH ASC PACK, kit number AGMM60M;   d)\tOUTPATIENT PORT ACCESS KIT  307907, kit number AHPO55J;   e)\tGeneral Pack, kit number BBGP31C;   f)\tFRACTURE TABLE PACK, kit number FDFT75N;   g)\tArthroscopy Pack, kit number HCAR04K;   h)\tBARIATRIC PACK, kit number HGBA92F;   i)\tLAPAROTOMY PACK, kit number HNLP12J;   j)\tMIDLINE CHANGE KIT, kit number HSMD20E;   k)\tMinor General, kit number JSMI10I;   l)\tENDO VASCULAR PACK, kit number LVEV61;   m)\tMAJOR PACK, kit number LVMJ21;   n)\tHEAD AND NECK PACK, kit number MMHN37F;   o)\tKIT, MINOR U BAR, kit number MMNU34E;   p)\tKIT, MAJOR  UNIVERSAL, kit number MMUN28E;   q)\tVAG PLASTY PACK, kit number OSVP16;   r)\tDR L MAJOR, kit number SALM40H;   s)\tDR L MAJOR, kit number SALM40I;   t)\tMINOR BASIN SAH, kit number SAMB25E;   u)\tMAJOR SAH, kit number SAMJ36G;   v)\tMINOR PACK, kit number SMMN65;   w)\tGeneral Pack, kit number THGN59D;   x)\tMINOR PACK, kit number TPMN15;   y)\tMAJOR UNIVERSAL PACK, kit number TPUN48",
  "description": "FDA recall Z-0825-2024 — American Contract Systems, Inc. is recalling Custom procedural convenience kits and trays, general & plastic surgery, labeled as:    a)\tBRACHY THERAPY PROCEDURE PAC, kit number AGBR90E;   b)\tBRACHY THERAPY PROCEDURE PAC, kit number AGBR90E;   c)\tMINI MINOR AGH ASC PACK, kit number AGMM60M;   d)\tOUTPATIENT PORT ACCESS KIT  307907, kit number AHPO55J;   e)\tGeneral Pack, kit number BBGP31C;   f)\tFRACTURE TABLE PACK, kit number FDFT75N;   g)\tArthroscopy Pack, kit number HCAR04K;   h)\tBARIATRIC PACK, kit number HGBA92F;   i)\tLAPAROTOMY PACK, kit number HNLP12J;   j)\tMIDLINE CHANGE KIT, kit number HSMD20E;   k)\tMinor General, kit number JSMI10I;   l)\tENDO VASCULAR PACK, kit number LVEV61;   m)\tMAJOR PACK, kit number LVMJ21;   n)\tHEAD AND NECK PACK, kit number MMHN37F;   o)\tKIT, MINOR U BAR, kit number MMNU34E;   p)\tKIT, MAJOR  UNIVERSAL, kit number MMUN28E;   q)\tVAG PLASTY PACK, kit number OSVP16;   r)\tDR L MAJOR, kit number SALM40H;   s)\tDR L MAJOR, kit number SALM40I;   t)\tMINOR BASIN SAH, kit number SAMB25E;   u)\tMAJOR SAH, kit number SAMJ36G;   v)\tMINOR PACK, kit number SMMN65;   w)\tGeneral Pack, kit number THGN59D;   x)\tMINOR PACK, kit number TPMN15;   y)\tMAJOR UNIVERSAL PACK, kit number TPUN48 (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/",
  "rdfs:isDefinedBy": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/vocab/agent-native",
  "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": {
      "@type": "schema:GovernmentOrganization",
      "name": "U.S. Food & Drug Administration"
    }
  },
  "sameAs": "https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=Z-0825-2024&lang=eng",
  "about": {
    "@type": "schema:MedicalDevice",
    "name": "Custom procedural convenience kits and trays, general & plastic surgery, labeled as:    a)\tBRACHY THERAPY PROCEDURE PAC, kit number AGBR90E;   b)\tBRACHY THERAPY PROCEDURE PAC, kit number AGBR90E;   c)\tMINI MINOR AGH ASC PACK, kit number AGMM60M;   d)\tOUTPATIENT PORT ACCESS KIT  307907, kit number AHPO55J;   e)\tGeneral Pack, kit number BBGP31C;   f)\tFRACTURE TABLE PACK, kit number FDFT75N;   g)\tArthroscopy Pack, kit number HCAR04K;   h)\tBARIATRIC PACK, kit number HGBA92F;   i)\tLAPAROTOMY PACK, kit number HNLP12J;   j)\tMIDLINE CHANGE KIT, kit number HSMD20E;   k)\tMinor General, kit number JSMI10I;   l)\tENDO VASCULAR PACK, kit number LVEV61;   m)\tMAJOR PACK, kit number LVMJ21;   n)\tHEAD AND NECK PACK, kit number MMHN37F;   o)\tKIT, MINOR U BAR, kit number MMNU34E;   p)\tKIT, MAJOR  UNIVERSAL, kit number MMUN28E;   q)\tVAG PLASTY PACK, kit number OSVP16;   r)\tDR L MAJOR, kit number SALM40H;   s)\tDR L MAJOR, kit number SALM40I;   t)\tMINOR BASIN SAH, kit number SAMB25E;   u)\tMAJOR SAH, kit number SAMJ36G;   v)\tMINOR PACK, kit number SMMN65;   w)\tGeneral Pack, kit number THGN59D;   x)\tMINOR PACK, kit number TPMN15;   y)\tMAJOR UNIVERSAL PACK, kit number TPUN48",
    "manufacturer": {
      "@type": "schema:Organization",
      "name": "American Contract Systems, Inc."
    }
  },
  "claims": [
    {
      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-0825-2024/enforcement-record",
      "@type": "schema:Claim",
      "name": "FDA recall Z-0825-2024: American Contract Systems, Inc. is recalling Custom procedural convenience kits and trays, general & plastic surgery, labeled as:    a)\tBRACHY THERAPY PROCEDURE PAC, kit number AGBR90E;   b)\tBRACHY THERAPY PROCEDURE PAC, kit number AGBR90E;   c)\tMINI MINOR AGH ASC PACK, kit number AGMM60M;   d)\tOUTPATIENT PORT ACCESS KIT  307907, kit number AHPO55J;   e)\tGeneral Pack, kit number BBGP31C;   f)\tFRACTURE TABLE PACK, kit number FDFT75N;   g)\tArthroscopy Pack, kit number HCAR04K;   h)\tBARIATRIC PACK, kit number HGBA92F;   i)\tLAPAROTOMY PACK, kit number HNLP12J;   j)\tMIDLINE CHANGE KIT, kit number HSMD20E;   k)\tMinor General, kit number JSMI10I;   l)\tENDO VASCULAR PACK, kit number LVEV61;   m)\tMAJOR PACK, kit number LVMJ21;   n)\tHEAD AND NECK PACK, kit number MMHN37F;   o)\tKIT, MINOR U BAR, kit number MMNU34E;   p)\tKIT, MAJOR  UNIVERSAL, kit number MMUN28E;   q)\tVAG PLASTY PACK, kit number OSVP16;   r)\tDR L MAJOR, kit number SALM40H;   s)\tDR L MAJOR, kit number SALM40I;   t)\tMINOR BASIN SAH, kit number SAMB25E;   u)\tMAJOR SAH, kit number SAMJ36G;   v)\tMINOR PACK, kit number SMMN65;   w)\tGeneral Pack, kit number THGN59D;   x)\tMINOR PACK, kit number TPMN15;   y)\tMAJOR UNIVERSAL PACK, kit number TPUN48",
      "text": "The FDA logged enforcement record Z-0825-2024: American Contract Systems, Inc. is voluntarily recalling Custom procedural convenience kits and trays, general & plastic surgery, labeled as:    a)\tBRACHY THERAPY PROCEDURE PAC, kit number AGBR90E;   b)\tBRACHY THERAPY PROCEDURE PAC, kit number AGBR90E;   c)\tMINI MINOR AGH ASC PACK, kit number AGMM60M;   d)\tOUTPATIENT PORT ACCESS KIT  307907, kit number AHPO55J;   e)\tGeneral Pack, kit number BBGP31C;   f)\tFRACTURE TABLE PACK, kit number FDFT75N;   g)\tArthroscopy Pack, kit number HCAR04K;   h)\tBARIATRIC PACK, kit number HGBA92F;   i)\tLAPAROTOMY PACK, kit number HNLP12J;   j)\tMIDLINE CHANGE KIT, kit number HSMD20E;   k)\tMinor General, kit number JSMI10I;   l)\tENDO VASCULAR PACK, kit number LVEV61;   m)\tMAJOR PACK, kit number LVMJ21;   n)\tHEAD AND NECK PACK, kit number MMHN37F;   o)\tKIT, MINOR U BAR, kit number MMNU34E;   p)\tKIT, MAJOR  UNIVERSAL, kit number MMUN28E;   q)\tVAG PLASTY PACK, kit number OSVP16;   r)\tDR L MAJOR, kit number SALM40H;   s)\tDR L MAJOR, kit number SALM40I;   t)\tMINOR BASIN SAH, kit number SAMB25E;   u)\tMAJOR SAH, kit number SAMJ36G;   v)\tMINOR PACK, kit number SMMN65;   w)\tGeneral Pack, kit number THGN59D;   x)\tMINOR PACK, kit number TPMN15;   y)\tMAJOR UNIVERSAL PACK, kit number TPUN48 — reason: During an internal investigation, ACS identified that several components were \"piggybacked\" to ACS trays and subjected to the ACS sterilization process. There is no supporting documentation stating the \"piggybacked\" components were assessed to determine if they were suitable for exposure to elevated temperatures for an extended period of time and further exposure to sterilization. As a result, the  piggybacked  components may (1) have a loss/lack of functionality, (2) loss of drug efficacy, if applicable, and (3) may have had higher than specified EO residuals.. Status: Ongoing — the recall is still being carried out.. Initiated 2023-11-29. Affected lots/codes: a) AGBR90E, UDI/DI 00191072036865, Lot Numbers:  959231, exp. 02/10/2024; 681221, exp. 11/15/2023; 721221, exp. 09/30/2023; 771221, exp. 08/147/2023; 827221, exp. 06/22/2023; 897221, exp. 04/13/2023;  b) AGMM60M, UDI/DI 00191072063786, Lot Numbers:  939231, exp. 03/02/2024; 638221, exp. 4528812/28/2023; 694221, exp. 11/02/2023; 734221, exp. 09/23/2023; 769221, exp. 08/19/2023;  c) AHPO55J, UDI/DI 00191072171566, Lot Numbers:  682221, exp. 11/14/2023; 661221, exp. 12/5/2023; 977231, exp. 1/23/2024; 945231, exp. 2/24/2024; 891231, exp. 4/19/2024;  d) BBGP31C, UDI/DI none, Lot Numbers:  687221, exp. 11/9/2023; 738221, exp. 9/19/2023; 805221, exp. 7/14/2023; 870221, exp. 5/10/2023;  e) FDFT75N, UDI/DI none, Lot Numbers:  773221, exp. 8/15/2023; 714221, exp. 10/13/2023; 990231, exp. 1/10/2024; 935231, exp. 3/6/2024; 890231, exp. 4/20/2024; 870231, exp. 5/10/2024;  f) HCAR04K, UDI/DI 00191072114174, Lot Numbers:  757221, exp. 08/31/2023;  g) HGBA92F, UDI/DI none, Lot Numbers:  757221, exp. 8/31/2023; 695221, exp. 11/1/2023; 635221, exp. 12/31/2023; h) HNLP12J, UDI/DI 00191072146274, Lot Numbers:  805221, exp. 7/14/2023; 742221, exp. 9/15/2023; 673221, exp. 11/23/2023; 924231, exp. 3/17/2024; i) HSMD20E, UDI/DI 00191072130068, Lot Numbers:  898221, exp. 4/12/2023; 772221, exp. 8/16/2023; 984231, exp. 1/16/2024; j) JSMI10I, UDI/DI none, Lot Numbers:  766221, exp. 08/22/2023;   k) LVEV61, UDI/DI 00191072033475, Lot Numbers:  678221, exp. 11/18/2023; 637221, exp. 12/29/2023; l) LVMJ21, UDI/DI 00191072139023, Lot Numbers:  833221, exp. 6/16/2023; 764221, exp. 8/24/2023; 717221, exp. 10/10/2023; 988231, exp. 1/12/2024; 954231, exp. 2/15/2024; m) MMHN37F, UDI/DI none, Lot Numbers:  639221, exp. 12/27/2023;  n) MMNU34E, UDI/DI none, Lot Numbers:  928231, exp. 3/13/2024; 889231, exp. 4/21/2024; o) MMUN28E, UDI/DI none, Lot Numbers:  889231, exp. 04/21/2024;  p) OSVP16, UDI/DI 00191072156570, Lot Numbers:  827221, exp. 6/17/2023;  q) OSVP16, UDI/DI 00191072170835, Lot Numbers:  700221, exp. 10/23/2023; 644221, exp. 12/4/2023; 987231, exp. 11/20/2023; r) SALM40H, UDI/DI none, Lot Numbers:  826221, exp. 6/23/2023; 888221, exp. 4/22/2023; s) SALM40I, UDI/DI none, Lot Numbers:  687221, exp. 11/9/2023; 756221, exp. 9/1/2023; 984231, exp. 1/16/2024;  t) SAMB25E, UDI/DI none, Lot Numbers:  843221, exp. 6/6/2023; 894221, exp. 4/16/2023; 871221, exp. 5/9/2023; 686221, exp. 11/10/2023; 758221, exp. 8/30/2023; 793221, exp. 7/26/2023; 974231, exp. 1/26/2024; u) SAMJ36G, UDI/DI none, Lot Numbers:  660221, exp. 12/6/2023; 704221, exp. 10/23/2023; 752221, exp. 9/5/2023; 800221, exp. 7/19/2023; v) SMMN65, UDI/DI 00191072188472, Lot Numbers:  969231, exp. 1/31/2024; 926231, exp. 3/15/2024; w) SMMN65, UDI/DI none, Lot Numbers:  919231, exp. 3/22/2024;  x) THGN59D, UDI/DI 00191072191069, Lot Numbers:  805221, exp. 7/14/2023; 721221, exp. 10/6/2023; y) TPMN15, UDI/DI 00191072171771, Lot Numbers:  737221, exp. 9/20/2023; 702221, exp. 10/25/2023; 664221, exp. 12/2/2023; 990231, exp. 1/10/2024; 960231, exp. 2/9/2024; 939231, exp. 3/2/2024; 903231, exp. 4/7/2024;  z) TPUN48, UDI/DI 00191072171832, Lot Numbers:  738221, exp. 9/19/2023; 688221, exp. 11/8/2023; 637221, exp. 12/29/2023; 967231, exp. 2/2/2024; 924231, exp. 3/17/2024. 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-0825-2024&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-0825-2024&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-0825-2024/fda-classification",
      "@type": "schema:Claim",
      "name": "FDA classified recall Z-0825-2024 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-0825-2024&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-0825-2024&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-0825-2024/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": [
    {
      "@type": "schema:ItemList",
      "name": "FDA recall details — Z-0825-2024",
      "numberOfItems": 9,
      "itemListElement": [
        {
          "@type": "schema:ListItem",
          "position": 1,
          "item": {
            "Field": "Recall number",
            "Value": "Z-0825-2024",
            "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": "American Contract Systems, Inc.",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 6,
          "item": {
            "Field": "Reason",
            "Value": "During an internal investigation, ACS identified that several components were \"piggybacked\" to ACS trays and subjected to the ACS sterilization process. There is no supporting documentation stating the \"piggybacked\" components were assessed to determine if they were suitable for exposure to elevated temperatures for an extended period of time and further exposure to sterilization. As a result, the  piggybacked  components may (1) have a loss/lack of functionality, (2) loss of drug efficacy, if applicable, and (3) may have had higher than specified EO residuals.",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 7,
          "item": {
            "Field": "Initiated",
            "Value": "2023-11-29",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 8,
          "item": {
            "Field": "Lot/code info",
            "Value": "a) AGBR90E, UDI/DI 00191072036865, Lot Numbers:  959231, exp. 02/10/2024; 681221, exp. 11/15/2023; 721221, exp. 09/30/2023; 771221, exp. 08/147/2023; 827221, exp. 06/22/2023; 897221, exp. 04/13/2023;  b) AGMM60M, UDI/DI 00191072063786, Lot Numbers:  939231, exp. 03/02/2024; 638221, exp. 4528812/28/2023; 694221, exp. 11/02/2023; 734221, exp. 09/23/2023; 769221, exp. 08/19/2023;  c) AHPO55J, UDI/DI 00191072171566, Lot Numbers:  682221, exp. 11/14/2023; 661221, exp. 12/5/2023; 977231, exp. 1/23/2024; 945231, exp. 2/24/2024; 891231, exp. 4/19/2024;  d) BBGP31C, UDI/DI none, Lot Numbers:  687221, exp. 11/9/2023; 738221, exp. 9/19/2023; 805221, exp. 7/14/2023; 870221, exp. 5/10/2023;  e) FDFT75N, UDI/DI none, Lot Numbers:  773221, exp. 8/15/2023; 714221, exp. 10/13/2023; 990231, exp. 1/10/2024; 935231, exp. 3/6/2024; 890231, exp. 4/20/2024; 870231, exp. 5/10/2024;  f) HCAR04K, UDI/DI 00191072114174, Lot Numbers:  757221, exp. 08/31/2023;  g) HGBA92F, UDI/DI none, Lot Numbers:  757221, exp. 8/31/2023; 695221, exp. 11/1/2023; 635221, exp. 12/31/2023; h) HNLP12J, UDI/DI 00191072146274, Lot Numbers:  805221, exp. 7/14/2023; 742221, exp. 9/15/2023; 673221, exp. 11/23/2023; 924231, exp. 3/17/2024; i) HSMD20E, UDI/DI 00191072130068, Lot Numbers:  898221, exp. 4/12/2023; 772221, exp. 8/16/2023; 984231, exp. 1/16/2024; j) JSMI10I, UDI/DI none, Lot Numbers:  766221, exp. 08/22/2023;   k) LVEV61, UDI/DI 00191072033475, Lot Numbers:  678221, exp. 11/18/2023; 637221, exp. 12/29/2023; l) LVMJ21, UDI/DI 00191072139023, Lot Numbers:  833221, exp. 6/16/2023; 764221, exp. 8/24/2023; 717221, exp. 10/10/2023; 988231, exp. 1/12/2024; 954231, exp. 2/15/2024; m) MMHN37F, UDI/DI none, Lot Numbers:  639221, exp. 12/27/2023;  n) MMNU34E, UDI/DI none, Lot Numbers:  928231, exp. 3/13/2024; 889231, exp. 4/21/2024; o) MMUN28E, UDI/DI none, Lot Numbers:  889231, exp. 04/21/2024;  p) OSVP16, UDI/DI 00191072156570, Lot Numbers:  827221, exp. 6/17/2023;  q) OSVP16, UDI/DI 00191072170835, Lot Numbers:  700221, exp. 10/23/2023; 644221, exp. 12/4/2023; 987231, exp. 11/20/2023; r) SALM40H, UDI/DI none, Lot Numbers:  826221, exp. 6/23/2023; 888221, exp. 4/22/2023; s) SALM40I, UDI/DI none, Lot Numbers:  687221, exp. 11/9/2023; 756221, exp. 9/1/2023; 984231, exp. 1/16/2024;  t) SAMB25E, UDI/DI none, Lot Numbers:  843221, exp. 6/6/2023; 894221, exp. 4/16/2023; 871221, exp. 5/9/2023; 686221, exp. 11/10/2023; 758221, exp. 8/30/2023; 793221, exp. 7/26/2023; 974231, exp. 1/26/2024; u) SAMJ36G, UDI/DI none, Lot Numbers:  660221, exp. 12/6/2023; 704221, exp. 10/23/2023; 752221, exp. 9/5/2023; 800221, exp. 7/19/2023; v) SMMN65, UDI/DI 00191072188472, Lot Numbers:  969231, exp. 1/31/2024; 926231, exp. 3/15/2024; w) SMMN65, UDI/DI none, Lot Numbers:  919231, exp. 3/22/2024;  x) THGN59D, UDI/DI 00191072191069, Lot Numbers:  805221, exp. 7/14/2023; 721221, exp. 10/6/2023; y) TPMN15, UDI/DI 00191072171771, Lot Numbers:  737221, exp. 9/20/2023; 702221, exp. 10/25/2023; 664221, exp. 12/2/2023; 990231, exp. 1/10/2024; 960231, exp. 2/9/2024; 939231, exp. 3/2/2024; 903231, exp. 4/7/2024;  z) TPUN48, UDI/DI 00191072171832, Lot Numbers:  738221, exp. 9/19/2023; 688221, exp. 11/8/2023; 637221, exp. 12/29/2023; 967231, exp. 2/2/2024; 924231, exp. 3/17/2024",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 9,
          "item": {
            "Field": "Distribution pattern",
            "Value": "US Nationwide distribution.",
            "Status": "recorded"
          }
        }
      ]
    }
  ]
}