{
  "@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-2251-2023.jsonld",
  "@type": "schema:Dataset",
  "name": "Equipment and table drapes and Surgical Room Turnover (SRT) Kits:    (1) Ecolab Absorbent Table Cover W/Transfer Sheet & Armboard Covers, Model #ABTSLSAN, 20/case, non-sterile;  (2) Microtek/Ecolab/CleanOp Absorbent Table Cover w/Transfer Sheet, Model ABTSLSN, 25/case, non-sterile;    Surgical Room Turnover (SRT) Kits:    (3) Ecolab Genesys CleanOp Infection Control System, Model ALHS-02, 12/case, non-sterile;  (4) Ecolab Genesys CleanOp Infection Control System, Model ALHS-SS-01, 12/case, non-sterile;  (5) Ecolab CleanOp Infection Control System, Model BPGN-02, 10/case, non-sterile;  (6) Ecolab Genesys CleanOp Infection Control System, Model HFH-02, 12/case, non-sterile;  (7) Ecolab Genesys CleanOp Infection Control System, Model HKHA-02, 15/case, non-sterile;  (8) Ecolab CleanOp Infection Control System, Model JFKSC-01, 15/case, non-sterile;  (9) Ecolab Genesys CleanOp Infection Control System, Model LH-LD-05, 12/case, non-sterile;  (10) Ecolab CleanOp Infection Control System, Model NEGM-CV-01D, 9/case, non-sterile;  (11) Ecolab Genesys CleanOp Infection Control System, Model PMMC-02D, 12/case, non-sterile;  (12) Ecolab Genesys CleanOp Infection Control System, Model PMMC-SP-01D, 12/case, non-sterile;  (13) Ecolab Genesys CleanOp Infection Control System, Model SHMC-06, 15/case, non-sterile;  (14) Ecolab CleanOp Infection Control System, Model SR-01D, 12/case, non-sterile;  (15) Ecolab CleanOp Infection Control System, Model SVB-OSC-01, 12/case, non-sterile;  (16) Ecolab CleanOp Infection Control System, Model UCLA-LD-03, 12/case, non-sterile;  (17) Ecolab CleanOp Infection Control System, Model VAIC-03, 12/case, non-sterile; and  (18) Ecolab Genesys CleanOp Infection Control System, Model VAIC-CP-02, 15/case, non-sterile.",
  "description": "FDA recall Z-2251-2023 — Microtek Medical Inc. is recalling Equipment and table drapes and Surgical Room Turnover (SRT) Kits:    (1) Ecolab Absorbent Table Cover W/Transfer Sheet & Armboard Covers, Model #ABTSLSAN, 20/case, non-sterile;  (2) Microtek/Ecolab/CleanOp Absorbent Table Cover w/Transfer Sheet, Model ABTSLSN, 25/case, non-sterile;    Surgical Room Turnover (SRT) Kits:    (3) Ecolab Genesys CleanOp Infection Control System, Model ALHS-02, 12/case, non-sterile;  (4) Ecolab Genesys CleanOp Infection Control System, Model ALHS-SS-01, 12/case, non-sterile;  (5) Ecolab CleanOp Infection Control System, Model BPGN-02, 10/case, non-sterile;  (6) Ecolab Genesys CleanOp Infection Control System, Model HFH-02, 12/case, non-sterile;  (7) Ecolab Genesys CleanOp Infection Control System, Model HKHA-02, 15/case, non-sterile;  (8) Ecolab CleanOp Infection Control System, Model JFKSC-01, 15/case, non-sterile;  (9) Ecolab Genesys CleanOp Infection Control System, Model LH-LD-05, 12/case, non-sterile;  (10) Ecolab CleanOp Infection Control System, Model NEGM-CV-01D, 9/case, non-sterile;  (11) Ecolab Genesys CleanOp Infection Control System, Model PMMC-02D, 12/case, non-sterile;  (12) Ecolab Genesys CleanOp Infection Control System, Model PMMC-SP-01D, 12/case, non-sterile;  (13) Ecolab Genesys CleanOp Infection Control System, Model SHMC-06, 15/case, non-sterile;  (14) Ecolab CleanOp Infection Control System, Model SR-01D, 12/case, non-sterile;  (15) Ecolab CleanOp Infection Control System, Model SVB-OSC-01, 12/case, non-sterile;  (16) Ecolab CleanOp Infection Control System, Model UCLA-LD-03, 12/case, non-sterile;  (17) Ecolab CleanOp Infection Control System, Model VAIC-03, 12/case, non-sterile; and  (18) Ecolab Genesys CleanOp Infection Control System, Model VAIC-CP-02, 15/case, non-sterile. (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-2251-2023&lang=eng",
  "about": {
    "@type": "schema:MedicalDevice",
    "name": "Equipment and table drapes and Surgical Room Turnover (SRT) Kits:    (1) Ecolab Absorbent Table Cover W/Transfer Sheet & Armboard Covers, Model #ABTSLSAN, 20/case, non-sterile;  (2) Microtek/Ecolab/CleanOp Absorbent Table Cover w/Transfer Sheet, Model ABTSLSN, 25/case, non-sterile;    Surgical Room Turnover (SRT) Kits:    (3) Ecolab Genesys CleanOp Infection Control System, Model ALHS-02, 12/case, non-sterile;  (4) Ecolab Genesys CleanOp Infection Control System, Model ALHS-SS-01, 12/case, non-sterile;  (5) Ecolab CleanOp Infection Control System, Model BPGN-02, 10/case, non-sterile;  (6) Ecolab Genesys CleanOp Infection Control System, Model HFH-02, 12/case, non-sterile;  (7) Ecolab Genesys CleanOp Infection Control System, Model HKHA-02, 15/case, non-sterile;  (8) Ecolab CleanOp Infection Control System, Model JFKSC-01, 15/case, non-sterile;  (9) Ecolab Genesys CleanOp Infection Control System, Model LH-LD-05, 12/case, non-sterile;  (10) Ecolab CleanOp Infection Control System, Model NEGM-CV-01D, 9/case, non-sterile;  (11) Ecolab Genesys CleanOp Infection Control System, Model PMMC-02D, 12/case, non-sterile;  (12) Ecolab Genesys CleanOp Infection Control System, Model PMMC-SP-01D, 12/case, non-sterile;  (13) Ecolab Genesys CleanOp Infection Control System, Model SHMC-06, 15/case, non-sterile;  (14) Ecolab CleanOp Infection Control System, Model SR-01D, 12/case, non-sterile;  (15) Ecolab CleanOp Infection Control System, Model SVB-OSC-01, 12/case, non-sterile;  (16) Ecolab CleanOp Infection Control System, Model UCLA-LD-03, 12/case, non-sterile;  (17) Ecolab CleanOp Infection Control System, Model VAIC-03, 12/case, non-sterile; and  (18) Ecolab Genesys CleanOp Infection Control System, Model VAIC-CP-02, 15/case, non-sterile.",
    "manufacturer": {
      "@type": "schema:Organization",
      "name": "Microtek Medical Inc."
    }
  },
  "claims": [
    {
      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-2251-2023/enforcement-record",
      "@type": "schema:Claim",
      "name": "FDA recall Z-2251-2023: Microtek Medical Inc. is recalling Equipment and table drapes and Surgical Room Turnover (SRT) Kits:    (1) Ecolab Absorbent Table Cover W/Transfer Sheet & Armboard Covers, Model #ABTSLSAN, 20/case, non-sterile;  (2) Microtek/Ecolab/CleanOp Absorbent Table Cover w/Transfer Sheet, Model ABTSLSN, 25/case, non-sterile;    Surgical Room Turnover (SRT) Kits:    (3) Ecolab Genesys CleanOp Infection Control System, Model ALHS-02, 12/case, non-sterile;  (4) Ecolab Genesys CleanOp Infection Control System, Model ALHS-SS-01, 12/case, non-sterile;  (5) Ecolab CleanOp Infection Control System, Model BPGN-02, 10/case, non-sterile;  (6) Ecolab Genesys CleanOp Infection Control System, Model HFH-02, 12/case, non-sterile;  (7) Ecolab Genesys CleanOp Infection Control System, Model HKHA-02, 15/case, non-sterile;  (8) Ecolab CleanOp Infection Control System, Model JFKSC-01, 15/case, non-sterile;  (9) Ecolab Genesys CleanOp Infection Control System, Model LH-LD-05, 12/case, non-sterile;  (10) Ecolab CleanOp Infection Control System, Model NEGM-CV-01D, 9/case, non-sterile;  (11) Ecolab Genesys CleanOp Infection Control System, Model PMMC-02D, 12/case, non-sterile;  (12) Ecolab Genesys CleanOp Infection Control System, Model PMMC-SP-01D, 12/case, non-sterile;  (13) Ecolab Genesys CleanOp Infection Control System, Model SHMC-06, 15/case, non-sterile;  (14) Ecolab CleanOp Infection Control System, Model SR-01D, 12/case, non-sterile;  (15) Ecolab CleanOp Infection Control System, Model SVB-OSC-01, 12/case, non-sterile;  (16) Ecolab CleanOp Infection Control System, Model UCLA-LD-03, 12/case, non-sterile;  (17) Ecolab CleanOp Infection Control System, Model VAIC-03, 12/case, non-sterile; and  (18) Ecolab Genesys CleanOp Infection Control System, Model VAIC-CP-02, 15/case, non-sterile.",
      "text": "The FDA logged enforcement record Z-2251-2023: Microtek Medical Inc. is voluntarily recalling Equipment and table drapes and Surgical Room Turnover (SRT) Kits:    (1) Ecolab Absorbent Table Cover W/Transfer Sheet & Armboard Covers, Model #ABTSLSAN, 20/case, non-sterile;  (2) Microtek/Ecolab/CleanOp Absorbent Table Cover w/Transfer Sheet, Model ABTSLSN, 25/case, non-sterile;    Surgical Room Turnover (SRT) Kits:    (3) Ecolab Genesys CleanOp Infection Control System, Model ALHS-02, 12/case, non-sterile;  (4) Ecolab Genesys CleanOp Infection Control System, Model ALHS-SS-01, 12/case, non-sterile;  (5) Ecolab CleanOp Infection Control System, Model BPGN-02, 10/case, non-sterile;  (6) Ecolab Genesys CleanOp Infection Control System, Model HFH-02, 12/case, non-sterile;  (7) Ecolab Genesys CleanOp Infection Control System, Model HKHA-02, 15/case, non-sterile;  (8) Ecolab CleanOp Infection Control System, Model JFKSC-01, 15/case, non-sterile;  (9) Ecolab Genesys CleanOp Infection Control System, Model LH-LD-05, 12/case, non-sterile;  (10) Ecolab CleanOp Infection Control System, Model NEGM-CV-01D, 9/case, non-sterile;  (11) Ecolab Genesys CleanOp Infection Control System, Model PMMC-02D, 12/case, non-sterile;  (12) Ecolab Genesys CleanOp Infection Control System, Model PMMC-SP-01D, 12/case, non-sterile;  (13) Ecolab Genesys CleanOp Infection Control System, Model SHMC-06, 15/case, non-sterile;  (14) Ecolab CleanOp Infection Control System, Model SR-01D, 12/case, non-sterile;  (15) Ecolab CleanOp Infection Control System, Model SVB-OSC-01, 12/case, non-sterile;  (16) Ecolab CleanOp Infection Control System, Model UCLA-LD-03, 12/case, non-sterile;  (17) Ecolab CleanOp Infection Control System, Model VAIC-03, 12/case, non-sterile; and  (18) Ecolab Genesys CleanOp Infection Control System, Model VAIC-CP-02, 15/case, non-sterile. — reason: Certain lots of the products have a Naphthalene odor.. Status: Ongoing — the recall is still being carried out.. Initiated 2023-06-23. Affected lots/codes: (1) Model ABTSLSAN - Lot numbers 220309D, exp 3/9/2027; and 220302D, exp 3/2/2027; UDI-DI 50748426077262; (2) Model ABTSLSN - Lot number 220301D, exp 3/1/2027; UDI-DI 50748426077255; (3) Model ALHS-02 - Lot numbers 1392JX0100, exp 9/1/2027; 2452JX3000, exp 11/1/2027; 3402JX2000, exp 10/1/2027; 4382JX0900, exp 9/1/2027; 4442JX1100, exp 11/1/2027; and 5422JX0100, 10/1/2027; UDI-DI 00748426133512; (4) Model ALHS-SS-01 - Lot number 6382JX1000, exp 9/1/2027; UDI-DI 00748426123131; (5) Model BPGN-02 - Lot numbers 2362JX2100, exp 9/1/2027;  and 5412JX3200, exp 10/1/2027; UDI-DI 00748426080021; (6) Model HFH-02 - Lot number 2362JX1000, exp 9/1/2027; UDI-DI 00748426124688; (7) Model HKHA-02 - Lot numbers 1372JX0400, exp 9/1/2027; and 3412JX0700, exp 10/1/2027; UDI-DI 00748426077809; (8) Model JFKSC-01 - Lot numbers 6372JX1200, exp 9/1/2027; and 6372JX1300, exp 9/1/2027; UDI-DI 00748426078417; (9) Model LH-LD-05 - Lot numbers 7372JX2400, exp 9/1/2027; and 2422JX1900, exp 10/1/2027; UDI-DI 00748426082803; (10) Model NEGM-CV-01D - Lot numbers 5322JX1100, exp 8/12/2027; and 2013JX3400, exp 1/3/2028; UDI-DI 00748426132034; (11) Model PMMC-02D - Lot numbers 2332JX0900, exp 8/1/2027; 3362JX1200, exp 9/1/2027; and 2422JX2200, 10/1/2027; UDI-DI 00748426132034; (12) Model PMMC-SP-01D - Lot numbers 6282JX2600, exp 7/1/2027; 7372JX1900, exp 9/1/2027; 2412JX2300, exp 10/1/2027; and 6432JX0500, 10/1/2027; UDI-DI 00748426125753; (13) Model SHMC-06 - Lot numbers 2342JX0100, exp 8/1/2027; 1372JX0200, exp 9/1/2027; 3402JX1300, exp 10/1/2027; 6422JX0700, exp 10/1/2027; 6442JX0100, exp 11/1/2027;  and 5312JX0100, exp 8/1/2027; UDI-DI 00748426068258; (14) Model SR-01D - Lot numbers 1362JX0300, exp 9/5/2027; and 5372JX0700, exp 9/16/2027; UDI-DI 00748426128723; (15) Model SVB-OSC-01 - Lot numbers 3392JX0100, exp 9/1/2027; and 2412JX3300, exp 10/1/2027; UDI-DI 00748426109326; (16) Model UCLA-LD-03 - Lot number 3382JX2100, exp 9/1/2027;  UDI-DI 00748426115228; (17) Model VAIC-03 - Lot numbers 3282JX2500, exp 7/1/2027; 1442JX0600, 10/1/2027; 2432JX1700, exp 10/1/2027; and 4023JX3100, 1/1/2028; UDI-DI 00748426078837; and (18) Model VAIC-CP-02 - Lot number 5332JX2100, exp 8/1/2027; UDI-DI 00748426078813.. 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-2251-2023&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-2251-2023&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-2251-2023/fda-classification",
      "@type": "schema:Claim",
      "name": "FDA classified recall Z-2251-2023 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-2251-2023&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-2251-2023&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-2251-2023/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-2251-2023",
      "numberOfItems": 9,
      "itemListElement": [
        {
          "@type": "schema:ListItem",
          "position": 1,
          "item": {
            "Field": "Recall number",
            "Value": "Z-2251-2023",
            "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": "Microtek Medical Inc.",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 6,
          "item": {
            "Field": "Reason",
            "Value": "Certain lots of the products have a Naphthalene odor.",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 7,
          "item": {
            "Field": "Initiated",
            "Value": "2023-06-23",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 8,
          "item": {
            "Field": "Lot/code info",
            "Value": "(1) Model ABTSLSAN - Lot numbers 220309D, exp 3/9/2027; and 220302D, exp 3/2/2027; UDI-DI 50748426077262; (2) Model ABTSLSN - Lot number 220301D, exp 3/1/2027; UDI-DI 50748426077255; (3) Model ALHS-02 - Lot numbers 1392JX0100, exp 9/1/2027; 2452JX3000, exp 11/1/2027; 3402JX2000, exp 10/1/2027; 4382JX0900, exp 9/1/2027; 4442JX1100, exp 11/1/2027; and 5422JX0100, 10/1/2027; UDI-DI 00748426133512; (4) Model ALHS-SS-01 - Lot number 6382JX1000, exp 9/1/2027; UDI-DI 00748426123131; (5) Model BPGN-02 - Lot numbers 2362JX2100, exp 9/1/2027;  and 5412JX3200, exp 10/1/2027; UDI-DI 00748426080021; (6) Model HFH-02 - Lot number 2362JX1000, exp 9/1/2027; UDI-DI 00748426124688; (7) Model HKHA-02 - Lot numbers 1372JX0400, exp 9/1/2027; and 3412JX0700, exp 10/1/2027; UDI-DI 00748426077809; (8) Model JFKSC-01 - Lot numbers 6372JX1200, exp 9/1/2027; and 6372JX1300, exp 9/1/2027; UDI-DI 00748426078417; (9) Model LH-LD-05 - Lot numbers 7372JX2400, exp 9/1/2027; and 2422JX1900, exp 10/1/2027; UDI-DI 00748426082803; (10) Model NEGM-CV-01D - Lot numbers 5322JX1100, exp 8/12/2027; and 2013JX3400, exp 1/3/2028; UDI-DI 00748426132034; (11) Model PMMC-02D - Lot numbers 2332JX0900, exp 8/1/2027; 3362JX1200, exp 9/1/2027; and 2422JX2200, 10/1/2027; UDI-DI 00748426132034; (12) Model PMMC-SP-01D - Lot numbers 6282JX2600, exp 7/1/2027; 7372JX1900, exp 9/1/2027; 2412JX2300, exp 10/1/2027; and 6432JX0500, 10/1/2027; UDI-DI 00748426125753; (13) Model SHMC-06 - Lot numbers 2342JX0100, exp 8/1/2027; 1372JX0200, exp 9/1/2027; 3402JX1300, exp 10/1/2027; 6422JX0700, exp 10/1/2027; 6442JX0100, exp 11/1/2027;  and 5312JX0100, exp 8/1/2027; UDI-DI 00748426068258; (14) Model SR-01D - Lot numbers 1362JX0300, exp 9/5/2027; and 5372JX0700, exp 9/16/2027; UDI-DI 00748426128723; (15) Model SVB-OSC-01 - Lot numbers 3392JX0100, exp 9/1/2027; and 2412JX3300, exp 10/1/2027; UDI-DI 00748426109326; (16) Model UCLA-LD-03 - Lot number 3382JX2100, exp 9/1/2027;  UDI-DI 00748426115228; (17) Model VAIC-03 - Lot numbers 3282JX2500, exp 7/1/2027; 1442JX0600, 10/1/2027; 2432JX1700, exp 10/1/2027; and 4023JX3100, 1/1/2028; UDI-DI 00748426078837; and (18) Model VAIC-CP-02 - Lot number 5332JX2100, exp 8/1/2027; UDI-DI 00748426078813.",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 9,
          "item": {
            "Field": "Distribution pattern",
            "Value": "Worldwide distribution - US Nationwide and the country of Canada.",
            "Status": "recorded"
          }
        }
      ]
    }
  ]
}