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  "@type": "schema:Dataset",
  "name": "Medline Convenience kits labeled as:    1) STEREOTACTIC BREAST BIOPSY TRA, Pack Number BT1095 ;   2) BREAST BIOPSY TRAY, Pack Number MNS5070;   3) BREAST BIOPSY TRAY-LF, Pack Number SPEC0058A;   4) BREAST BIOPSY TRAY, Pack Number DYNDH1142A;   5) BREAST BIOPSY TRAY, Pack Number SPEC0130B;   6) BIOPSY PACK SM, Pack Number DYNDH1093;   7) HOLSTON MYELOGRAM PACK, Pack Number DYNDH1227A;   8) MAMMOGRAPHY BIOPSY TRAY, Pack Number DYNDH1304A;   9) LACERATION TRAY, Pack Number DYNDL1250C;   10) PULL D/C PACK, Pack Number DYNDA2080;   11) DIAGNOSTIC TRAY, Pack Number DYNDH1359;   12) OB DELIVERY SET, Pack Number MNS3355;   13) SUTURING SET, Pack Number SUT4020;   14) 22G FACET TRAY, Pack Number SPEC0265A;   15) ARTHROGRAM TRAY, Pack Number DYNDH1349;   16) BIOPSY TRAY W/O LIDOCAINE, Pack Number SPEC0196B;   17) ULTRASOUND BREAST BIOPSY, Pack Number DYNDH1496;   18) BREAST BIOPSY TRAY, Pack Number SPEC0130C;   19) DELIVERY ACCESSORY KIT, Pack Number MNS6496;   20) BREAST BIOPSY KIT, Pack Number DYNDH1706;   21) BIOPSY TRAY - LF, Pack Number DYNJTS0018A;   22) STEREO PROCEDURE TRAY, Pack Number DYNDC2859A;   23) STEREOTACTIC BREAST BIOPSY TRAY, Pack Number DYNDH1755;   24) BREAST BIOPSY, Pack Number DYNDH1518A;   25) PORT INSERTION KIT, Pack Number MNS11590;   26) CORE BIOPSY TRAY, Pack Number SPEC0083B;   27) INFUSION CENTER BLOOD DRAW KIT, Pack Number DYNDH1798;   28) BREAST CENTER BIOPSY TRAY, Pack Number DYNDH1519;   29) AULTMAN HOSPITAL CHEST TUBE INSERTION TR, Pack Number CHT500;   30) BREAST BIOPSY TRAY, Pack Number DYNDH1257;   31) ARTHROGRAM TRAY, Pack Number DYNDH1134;   32) ULTRASOUND GUIDE BREAST BIOPSY, Pack Number DYNDH1319;   33) BIOPSY TRAY, Pack Number DYNDH1269;   34) BIOPSY BASIC PACK, Pack Number DYNDH1588",
  "description": "FDA recall Z-3030-2024 — MEDLINE INDUSTRIES, LP - Northfield is recalling Medline Convenience kits labeled as:    1) STEREOTACTIC BREAST BIOPSY TRA, Pack Number BT1095 ;   2) BREAST BIOPSY TRAY, Pack Number MNS5070;   3) BREAST BIOPSY TRAY-LF, Pack Number SPEC0058A;   4) BREAST BIOPSY TRAY, Pack Number DYNDH1142A;   5) BREAST BIOPSY TRAY, Pack Number SPEC0130B;   6) BIOPSY PACK SM, Pack Number DYNDH1093;   7) HOLSTON MYELOGRAM PACK, Pack Number DYNDH1227A;   8) MAMMOGRAPHY BIOPSY TRAY, Pack Number DYNDH1304A;   9) LACERATION TRAY, Pack Number DYNDL1250C;   10) PULL D/C PACK, Pack Number DYNDA2080;   11) DIAGNOSTIC TRAY, Pack Number DYNDH1359;   12) OB DELIVERY SET, Pack Number MNS3355;   13) SUTURING SET, Pack Number SUT4020;   14) 22G FACET TRAY, Pack Number SPEC0265A;   15) ARTHROGRAM TRAY, Pack Number DYNDH1349;   16) BIOPSY TRAY W/O LIDOCAINE, Pack Number SPEC0196B;   17) ULTRASOUND BREAST BIOPSY, Pack Number DYNDH1496;   18) BREAST BIOPSY TRAY, Pack Number SPEC0130C;   19) DELIVERY ACCESSORY KIT, Pack Number MNS6496;   20) BREAST BIOPSY KIT, Pack Number DYNDH1706;   21) BIOPSY TRAY - LF, Pack Number DYNJTS0018A;   22) STEREO PROCEDURE TRAY, Pack Number DYNDC2859A;   23) STEREOTACTIC BREAST BIOPSY TRAY, Pack Number DYNDH1755;   24) BREAST BIOPSY, Pack Number DYNDH1518A;   25) PORT INSERTION KIT, Pack Number MNS11590;   26) CORE BIOPSY TRAY, Pack Number SPEC0083B;   27) INFUSION CENTER BLOOD DRAW KIT, Pack Number DYNDH1798;   28) BREAST CENTER BIOPSY TRAY, Pack Number DYNDH1519;   29) AULTMAN HOSPITAL CHEST TUBE INSERTION TR, Pack Number CHT500;   30) BREAST BIOPSY TRAY, Pack Number DYNDH1257;   31) ARTHROGRAM TRAY, Pack Number DYNDH1134;   32) ULTRASOUND GUIDE BREAST BIOPSY, Pack Number DYNDH1319;   33) BIOPSY TRAY, Pack Number DYNDH1269;   34) BIOPSY BASIC PACK, Pack Number DYNDH1588 (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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    "@type": "schema:MedicalDevice",
    "name": "Medline Convenience kits labeled as:    1) STEREOTACTIC BREAST BIOPSY TRA, Pack Number BT1095 ;   2) BREAST BIOPSY TRAY, Pack Number MNS5070;   3) BREAST BIOPSY TRAY-LF, Pack Number SPEC0058A;   4) BREAST BIOPSY TRAY, Pack Number DYNDH1142A;   5) BREAST BIOPSY TRAY, Pack Number SPEC0130B;   6) BIOPSY PACK SM, Pack Number DYNDH1093;   7) HOLSTON MYELOGRAM PACK, Pack Number DYNDH1227A;   8) MAMMOGRAPHY BIOPSY TRAY, Pack Number DYNDH1304A;   9) LACERATION TRAY, Pack Number DYNDL1250C;   10) PULL D/C PACK, Pack Number DYNDA2080;   11) DIAGNOSTIC TRAY, Pack Number DYNDH1359;   12) OB DELIVERY SET, Pack Number MNS3355;   13) SUTURING SET, Pack Number SUT4020;   14) 22G FACET TRAY, Pack Number SPEC0265A;   15) ARTHROGRAM TRAY, Pack Number DYNDH1349;   16) BIOPSY TRAY W/O LIDOCAINE, Pack Number SPEC0196B;   17) ULTRASOUND BREAST BIOPSY, Pack Number DYNDH1496;   18) BREAST BIOPSY TRAY, Pack Number SPEC0130C;   19) DELIVERY ACCESSORY KIT, Pack Number MNS6496;   20) BREAST BIOPSY KIT, Pack Number DYNDH1706;   21) BIOPSY TRAY - LF, Pack Number DYNJTS0018A;   22) STEREO PROCEDURE TRAY, Pack Number DYNDC2859A;   23) STEREOTACTIC BREAST BIOPSY TRAY, Pack Number DYNDH1755;   24) BREAST BIOPSY, Pack Number DYNDH1518A;   25) PORT INSERTION KIT, Pack Number MNS11590;   26) CORE BIOPSY TRAY, Pack Number SPEC0083B;   27) INFUSION CENTER BLOOD DRAW KIT, Pack Number DYNDH1798;   28) BREAST CENTER BIOPSY TRAY, Pack Number DYNDH1519;   29) AULTMAN HOSPITAL CHEST TUBE INSERTION TR, Pack Number CHT500;   30) BREAST BIOPSY TRAY, Pack Number DYNDH1257;   31) ARTHROGRAM TRAY, Pack Number DYNDH1134;   32) ULTRASOUND GUIDE BREAST BIOPSY, Pack Number DYNDH1319;   33) BIOPSY TRAY, Pack Number DYNDH1269;   34) BIOPSY BASIC PACK, Pack Number DYNDH1588",
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      "name": "MEDLINE INDUSTRIES, LP - Northfield"
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      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-3030-2024/enforcement-record",
      "@type": "schema:Claim",
      "name": "FDA recall Z-3030-2024: MEDLINE INDUSTRIES, LP - Northfield is recalling Medline Convenience kits labeled as:    1) STEREOTACTIC BREAST BIOPSY TRA, Pack Number BT1095 ;   2) BREAST BIOPSY TRAY, Pack Number MNS5070;   3) BREAST BIOPSY TRAY-LF, Pack Number SPEC0058A;   4) BREAST BIOPSY TRAY, Pack Number DYNDH1142A;   5) BREAST BIOPSY TRAY, Pack Number SPEC0130B;   6) BIOPSY PACK SM, Pack Number DYNDH1093;   7) HOLSTON MYELOGRAM PACK, Pack Number DYNDH1227A;   8) MAMMOGRAPHY BIOPSY TRAY, Pack Number DYNDH1304A;   9) LACERATION TRAY, Pack Number DYNDL1250C;   10) PULL D/C PACK, Pack Number DYNDA2080;   11) DIAGNOSTIC TRAY, Pack Number DYNDH1359;   12) OB DELIVERY SET, Pack Number MNS3355;   13) SUTURING SET, Pack Number SUT4020;   14) 22G FACET TRAY, Pack Number SPEC0265A;   15) ARTHROGRAM TRAY, Pack Number DYNDH1349;   16) BIOPSY TRAY W/O LIDOCAINE, Pack Number SPEC0196B;   17) ULTRASOUND BREAST BIOPSY, Pack Number DYNDH1496;   18) BREAST BIOPSY TRAY, Pack Number SPEC0130C;   19) DELIVERY ACCESSORY KIT, Pack Number MNS6496;   20) BREAST BIOPSY KIT, Pack Number DYNDH1706;   21) BIOPSY TRAY - LF, Pack Number DYNJTS0018A;   22) STEREO PROCEDURE TRAY, Pack Number DYNDC2859A;   23) STEREOTACTIC BREAST BIOPSY TRAY, Pack Number DYNDH1755;   24) BREAST BIOPSY, Pack Number DYNDH1518A;   25) PORT INSERTION KIT, Pack Number MNS11590;   26) CORE BIOPSY TRAY, Pack Number SPEC0083B;   27) INFUSION CENTER BLOOD DRAW KIT, Pack Number DYNDH1798;   28) BREAST CENTER BIOPSY TRAY, Pack Number DYNDH1519;   29) AULTMAN HOSPITAL CHEST TUBE INSERTION TR, Pack Number CHT500;   30) BREAST BIOPSY TRAY, Pack Number DYNDH1257;   31) ARTHROGRAM TRAY, Pack Number DYNDH1134;   32) ULTRASOUND GUIDE BREAST BIOPSY, Pack Number DYNDH1319;   33) BIOPSY TRAY, Pack Number DYNDH1269;   34) BIOPSY BASIC PACK, Pack Number DYNDH1588",
      "text": "The FDA logged enforcement record Z-3030-2024: MEDLINE INDUSTRIES, LP - Northfield is voluntarily recalling Medline Convenience kits labeled as:    1) STEREOTACTIC BREAST BIOPSY TRA, Pack Number BT1095 ;   2) BREAST BIOPSY TRAY, Pack Number MNS5070;   3) BREAST BIOPSY TRAY-LF, Pack Number SPEC0058A;   4) BREAST BIOPSY TRAY, Pack Number DYNDH1142A;   5) BREAST BIOPSY TRAY, Pack Number SPEC0130B;   6) BIOPSY PACK SM, Pack Number DYNDH1093;   7) HOLSTON MYELOGRAM PACK, Pack Number DYNDH1227A;   8) MAMMOGRAPHY BIOPSY TRAY, Pack Number DYNDH1304A;   9) LACERATION TRAY, Pack Number DYNDL1250C;   10) PULL D/C PACK, Pack Number DYNDA2080;   11) DIAGNOSTIC TRAY, Pack Number DYNDH1359;   12) OB DELIVERY SET, Pack Number MNS3355;   13) SUTURING SET, Pack Number SUT4020;   14) 22G FACET TRAY, Pack Number SPEC0265A;   15) ARTHROGRAM TRAY, Pack Number DYNDH1349;   16) BIOPSY TRAY W/O LIDOCAINE, Pack Number SPEC0196B;   17) ULTRASOUND BREAST BIOPSY, Pack Number DYNDH1496;   18) BREAST BIOPSY TRAY, Pack Number SPEC0130C;   19) DELIVERY ACCESSORY KIT, Pack Number MNS6496;   20) BREAST BIOPSY KIT, Pack Number DYNDH1706;   21) BIOPSY TRAY - LF, Pack Number DYNJTS0018A;   22) STEREO PROCEDURE TRAY, Pack Number DYNDC2859A;   23) STEREOTACTIC BREAST BIOPSY TRAY, Pack Number DYNDH1755;   24) BREAST BIOPSY, Pack Number DYNDH1518A;   25) PORT INSERTION KIT, Pack Number MNS11590;   26) CORE BIOPSY TRAY, Pack Number SPEC0083B;   27) INFUSION CENTER BLOOD DRAW KIT, Pack Number DYNDH1798;   28) BREAST CENTER BIOPSY TRAY, Pack Number DYNDH1519;   29) AULTMAN HOSPITAL CHEST TUBE INSERTION TR, Pack Number CHT500;   30) BREAST BIOPSY TRAY, Pack Number DYNDH1257;   31) ARTHROGRAM TRAY, Pack Number DYNDH1134;   32) ULTRASOUND GUIDE BREAST BIOPSY, Pack Number DYNDH1319;   33) BIOPSY TRAY, Pack Number DYNDH1269;   34) BIOPSY BASIC PACK, Pack Number DYNDH1588 — reason: Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.. Status: Ongoing — the recall is still being carried out.. Initiated 2024-04-08. Affected lots/codes: BT1095 , Lot Number 21HBO851 ;  BT1095 , Lot Number 21JBA498 ;  BT1095 , Lot Number 21KBS041 ;  BT1095 , Lot Number 21LBI316 ;  BT1095 , Lot Number 22IBE255 ;  BT1095 , Lot Number 23CBL036 ;  BT1095 , Lot Number 23DBE633 ;  BT1095 , Lot Number 21ABU603 ;   MNS5070, Lot Number 23LBC489;  MNS5070, Lot Number 23HBL700;  MNS5070, Lot Number 23EBJ365;  SPEC0058A, Lot Number 2018110290;  DYNDH1142A, Lot Number 2018120590;  SPEC0130B, Lot Number 2018121290;  SPEC0058A, Lot Number 2019012490;  DYNDH1093, Lot Number 2019012490;  SPEC0130B, Lot Number 2019020590;  DYNDH1227A, Lot Number 2019020590;  DYNDH1304A, Lot Number 2019040990;  DYNDL1250C, Lot Number 2019040990;  DYNDH1227A, Lot Number 2019040990;  DYNDL1250C, Lot Number 2019040990;  DYNDA2080, Lot Number 2019040990;  SPEC0058A, Lot Number 2019060690;  SPEC0130B, Lot Number 2019062890;  SPEC0058A, Lot Number 2019070290;  DYNDH1359, Lot Number 2019070290;  MNS3355, Lot Number 2019062890;  SPEC0130B, Lot Number 2019081590;  SUT4020, Lot Number 2019081590;  SPEC0265A, Lot Number 2019081590;  DYNDH1349, Lot Number 2019081590;  DYNDH1304A, Lot Number 2019112190;  SPEC0196B, Lot Number 2019112190;  DYNDH1349, Lot Number 2019112190;  SPEC0130B, Lot Number 2019121190;  DYNDH1496, Lot Number 2019122790;  DYNDH1496, Lot Number 2020013190;  DYNDH1496, Lot Number 2020120290;  DYNDH1496, Lot Number 2021022590;  SPEC0130C, Lot Number 2021051890;  MNS6496, Lot Number 2021051890;  SPEC0130C, Lot Number 2021071290;  SPEC0130C, Lot Number 2021082490;  SPEC0130C, Lot Number 2021091390;  DYNDH1706, Lot Number 2022021550;  SPEC0130C, Lot Number 2022020290;  SPEC0130C, Lot Number 2022032990;  DYNJTS0018A, Lot Number 2022032990;  DYNDC2859A, Lot Number 2022032990;  DYNDH1755, Lot Number 2022061050;  DYNDH1518A, Lot Number 2022061050;  SPEC0130C, Lot Number 2022081690;  SPEC0130C, Lot Number 2022120290;  MNS11590, Lot Number 2022120290;  SPEC0083B, Lot Number 2022120290;  DYNDH1798, Lot Number 2022120290;  DYNDH1519, Lot Number 2022120690;  CHT500, Lot Number 2022120690;  DYNDH1519, Lot Number 2023020390;  SPEC0130C, Lot Number 2023053190;  DYNDH1519, Lot Number 2023081590;  DYNDH1257, Lot Number 2018072450;  DYNDH1257, Lot Number 2018080950;  DYNDH1257, Lot Number 2018100350;  DYNDH1257, Lot Number 2018113050;  DYNDH1134, Lot Number 2018113050;  DYNDH1319, Lot Number 2019011750;  DYNDH1257, Lot Number 2019032150;  DYNDH1319, Lot Number 2019073050;  DYNDH1319, Lot Number 2019093050;  DYNDH1319, Lot Number 2019103150;  DYNDH1257, Lot Number 2020020350;  DYNDH1257, Lot Number 2020033150;  DYNDH1319, Lot Number 2020072050;  DYNDH1269, Lot Number 2020072050;  DYNDH1257, Lot Number 2020102950;  DYNDH1319, Lot Number 2021021950;  DYNDH1257, Lot Number 2021030350;  DYNDH1257, Lot Number 2021120750;  DYNDH1257, Lot Number 2022051350;  DYNDH1319, Lot Number 2022052650;  DYNDH1588, Lot Number 2022052650. 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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      "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-3030-2024&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-3030-2024&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-3030-2024/fda-classification",
      "@type": "schema:Claim",
      "name": "FDA classified recall Z-3030-2024 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-3030-2024&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-3030-2024&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-3030-2024/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-3030-2024",
      "numberOfItems": 9,
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          "position": 1,
          "item": {
            "Field": "Recall number",
            "Value": "Z-3030-2024",
            "Status": "recorded"
          }
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          "@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": "MEDLINE INDUSTRIES, LP - Northfield",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 6,
          "item": {
            "Field": "Reason",
            "Value": "Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.",
            "Status": "recorded"
          }
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          "item": {
            "Field": "Initiated",
            "Value": "2024-04-08",
            "Status": "recorded"
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          "item": {
            "Field": "Lot/code info",
            "Value": "BT1095 , Lot Number 21HBO851 ;  BT1095 , Lot Number 21JBA498 ;  BT1095 , Lot Number 21KBS041 ;  BT1095 , Lot Number 21LBI316 ;  BT1095 , Lot Number 22IBE255 ;  BT1095 , Lot Number 23CBL036 ;  BT1095 , Lot Number 23DBE633 ;  BT1095 , Lot Number 21ABU603 ;   MNS5070, Lot Number 23LBC489;  MNS5070, Lot Number 23HBL700;  MNS5070, Lot Number 23EBJ365;  SPEC0058A, Lot Number 2018110290;  DYNDH1142A, Lot Number 2018120590;  SPEC0130B, Lot Number 2018121290;  SPEC0058A, Lot Number 2019012490;  DYNDH1093, Lot Number 2019012490;  SPEC0130B, Lot Number 2019020590;  DYNDH1227A, Lot Number 2019020590;  DYNDH1304A, Lot Number 2019040990;  DYNDL1250C, Lot Number 2019040990;  DYNDH1227A, Lot Number 2019040990;  DYNDL1250C, Lot Number 2019040990;  DYNDA2080, Lot Number 2019040990;  SPEC0058A, Lot Number 2019060690;  SPEC0130B, Lot Number 2019062890;  SPEC0058A, Lot Number 2019070290;  DYNDH1359, Lot Number 2019070290;  MNS3355, Lot Number 2019062890;  SPEC0130B, Lot Number 2019081590;  SUT4020, Lot Number 2019081590;  SPEC0265A, Lot Number 2019081590;  DYNDH1349, Lot Number 2019081590;  DYNDH1304A, Lot Number 2019112190;  SPEC0196B, Lot Number 2019112190;  DYNDH1349, Lot Number 2019112190;  SPEC0130B, Lot Number 2019121190;  DYNDH1496, Lot Number 2019122790;  DYNDH1496, Lot Number 2020013190;  DYNDH1496, Lot Number 2020120290;  DYNDH1496, Lot Number 2021022590;  SPEC0130C, Lot Number 2021051890;  MNS6496, Lot Number 2021051890;  SPEC0130C, Lot Number 2021071290;  SPEC0130C, Lot Number 2021082490;  SPEC0130C, Lot Number 2021091390;  DYNDH1706, Lot Number 2022021550;  SPEC0130C, Lot Number 2022020290;  SPEC0130C, Lot Number 2022032990;  DYNJTS0018A, Lot Number 2022032990;  DYNDC2859A, Lot Number 2022032990;  DYNDH1755, Lot Number 2022061050;  DYNDH1518A, Lot Number 2022061050;  SPEC0130C, Lot Number 2022081690;  SPEC0130C, Lot Number 2022120290;  MNS11590, Lot Number 2022120290;  SPEC0083B, Lot Number 2022120290;  DYNDH1798, Lot Number 2022120290;  DYNDH1519, Lot Number 2022120690;  CHT500, Lot Number 2022120690;  DYNDH1519, Lot Number 2023020390;  SPEC0130C, Lot Number 2023053190;  DYNDH1519, Lot Number 2023081590;  DYNDH1257, Lot Number 2018072450;  DYNDH1257, Lot Number 2018080950;  DYNDH1257, Lot Number 2018100350;  DYNDH1257, Lot Number 2018113050;  DYNDH1134, Lot Number 2018113050;  DYNDH1319, Lot Number 2019011750;  DYNDH1257, Lot Number 2019032150;  DYNDH1319, Lot Number 2019073050;  DYNDH1319, Lot Number 2019093050;  DYNDH1319, Lot Number 2019103150;  DYNDH1257, Lot Number 2020020350;  DYNDH1257, Lot Number 2020033150;  DYNDH1319, Lot Number 2020072050;  DYNDH1269, Lot Number 2020072050;  DYNDH1257, Lot Number 2020102950;  DYNDH1319, Lot Number 2021021950;  DYNDH1257, Lot Number 2021030350;  DYNDH1257, Lot Number 2021120750;  DYNDH1257, Lot Number 2022051350;  DYNDH1319, Lot Number 2022052650;  DYNDH1588, Lot Number 2022052650",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 9,
          "item": {
            "Field": "Distribution pattern",
            "Value": "Worldwide distribution.",
            "Status": "recorded"
          }
        }
      ]
    }
  ]
}