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  "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-1437-2025.jsonld",
  "@type": "schema:Dataset",
  "name": "Medline procedure kits labeled as:    1) ANGIO DRAPE PACK (DRLUL)-LF, Pack Number DYNJ47718D;   2) ANGIO PACK, Pack Number DYNJ69678;   3) ANGIOGRAPHY CV RAD PACK, Pack Number DYNJ64936A;   4) ANGIOGRAPHY DRAPE PACK, Pack Number DYNJ49621C;   5) ANGIOGRAPHY PACK, Pack Number DYNJ61266A;   6) ANGIOGRAPHY PACK-LF, Pack Number DYNJ35916N;   7) ARTERIOGRAM PACK, Pack Number DYNJ34442F;   8) CARDIAC CATH FEMORAL PACK, Pack Number DYNJ53588I;   9) CARDIAC CATH PACK, Pack Number DYNJ31733C;   10) CARDIAC CATH PACK, Pack Number DYNJ41315A;   11) CARDIAC CATH PACK-LF, Pack Number DYNJ0380198L;   12) CATH LAB PACK, Pack Number 0M-CP31796Q;   13) CATH LAB PACK-LF, Pack Number DYNJ0194968AG;   14) CATH LAB TRAY, Pack Number 00-401610J;   15) CHRISTUS SR CATH LAB PACK, Pack Number DYNJ60931C;   16) CRMC CATH LAB TRAY JUDKINS-LF, Pack Number DYNJ61088F;   17) CRMC NEURO ENDO HYBRID-LF, Pack Number DYNJ61101D;   18) EP PACK MORNINGSIDE, Pack Number DYNJ69301;   19) FEMORAL TRAY 2, Pack Number DYNJ68812C;   20) INTERVENTIONAL MINOR PACK, Pack Number DYNJ24615D;   21) INTERVENTIONAL PACK, Pack Number DYNJ54253;   22) INTERVENTIONAL RADIOLOGY PK-LF, Pack Number PHS605358025B;   23) MORNINGSIDE CARDIAC CATH, Pack Number DYNJ58339A;   24) OR INTERVENTIONAL PACK, Pack Number DYNJ46934A;   25) PACK,CARDIAC CATH, Pack Number DYNJ65481;   26) PK, RADIOLOGY-SPECIALS, Pack Number DYNJ59628C;   27) PTCA TRAY-LF, Pack Number DYNJ07252V;   28) RADIOLOGY PACK, Pack Number DYNJ45393A;   29) RR-ANGIOGRAPHY DRAPE PACK-LF, Pack Number DYNJ0608549M;   30) SPEC ANGIO PACK (SASJK)642-LF, Pack Number DYNJ47586F;   31) SPECIALS LINE PACK, Pack Number DYNJ69504;   32) TV-CARDIAC CATH PACK-LF, Pack Number DYNJ41564P;   33) TV-CARDIAC CATH PACK-LF, Pack Number DYNJ41564P;   34) UTHET TYLER ELECTROPHYSIOLOGY, Pack Number DYNJ68672C",
  "description": "FDA recall Z-1437-2025 — MEDLINE INDUSTRIES, LP - Northfield is recalling Medline procedure kits labeled as:    1) ANGIO DRAPE PACK (DRLUL)-LF, Pack Number DYNJ47718D;   2) ANGIO PACK, Pack Number DYNJ69678;   3) ANGIOGRAPHY CV RAD PACK, Pack Number DYNJ64936A;   4) ANGIOGRAPHY DRAPE PACK, Pack Number DYNJ49621C;   5) ANGIOGRAPHY PACK, Pack Number DYNJ61266A;   6) ANGIOGRAPHY PACK-LF, Pack Number DYNJ35916N;   7) ARTERIOGRAM PACK, Pack Number DYNJ34442F;   8) CARDIAC CATH FEMORAL PACK, Pack Number DYNJ53588I;   9) CARDIAC CATH PACK, Pack Number DYNJ31733C;   10) CARDIAC CATH PACK, Pack Number DYNJ41315A;   11) CARDIAC CATH PACK-LF, Pack Number DYNJ0380198L;   12) CATH LAB PACK, Pack Number 0M-CP31796Q;   13) CATH LAB PACK-LF, Pack Number DYNJ0194968AG;   14) CATH LAB TRAY, Pack Number 00-401610J;   15) CHRISTUS SR CATH LAB PACK, Pack Number DYNJ60931C;   16) CRMC CATH LAB TRAY JUDKINS-LF, Pack Number DYNJ61088F;   17) CRMC NEURO ENDO HYBRID-LF, Pack Number DYNJ61101D;   18) EP PACK MORNINGSIDE, Pack Number DYNJ69301;   19) FEMORAL TRAY 2, Pack Number DYNJ68812C;   20) INTERVENTIONAL MINOR PACK, Pack Number DYNJ24615D;   21) INTERVENTIONAL PACK, Pack Number DYNJ54253;   22) INTERVENTIONAL RADIOLOGY PK-LF, Pack Number PHS605358025B;   23) MORNINGSIDE CARDIAC CATH, Pack Number DYNJ58339A;   24) OR INTERVENTIONAL PACK, Pack Number DYNJ46934A;   25) PACK,CARDIAC CATH, Pack Number DYNJ65481;   26) PK, RADIOLOGY-SPECIALS, Pack Number DYNJ59628C;   27) PTCA TRAY-LF, Pack Number DYNJ07252V;   28) RADIOLOGY PACK, Pack Number DYNJ45393A;   29) RR-ANGIOGRAPHY DRAPE PACK-LF, Pack Number DYNJ0608549M;   30) SPEC ANGIO PACK (SASJK)642-LF, Pack Number DYNJ47586F;   31) SPECIALS LINE PACK, Pack Number DYNJ69504;   32) TV-CARDIAC CATH PACK-LF, Pack Number DYNJ41564P;   33) TV-CARDIAC CATH PACK-LF, Pack Number DYNJ41564P;   34) UTHET TYLER ELECTROPHYSIOLOGY, Pack Number DYNJ68672C (Devices, Class II). The enforcement record is RECORDED; the classification is a DETERMINATION (FDA's regulatory verdict); the boundary is INTERPRETATION (a recall ≠ harm to a specific person). Source: openFDA. CC0.",
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  "dateModified": "2026-06-24T07:02:03.626072+00:00",
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  "about": {
    "@type": "schema:MedicalDevice",
    "name": "Medline procedure kits labeled as:    1) ANGIO DRAPE PACK (DRLUL)-LF, Pack Number DYNJ47718D;   2) ANGIO PACK, Pack Number DYNJ69678;   3) ANGIOGRAPHY CV RAD PACK, Pack Number DYNJ64936A;   4) ANGIOGRAPHY DRAPE PACK, Pack Number DYNJ49621C;   5) ANGIOGRAPHY PACK, Pack Number DYNJ61266A;   6) ANGIOGRAPHY PACK-LF, Pack Number DYNJ35916N;   7) ARTERIOGRAM PACK, Pack Number DYNJ34442F;   8) CARDIAC CATH FEMORAL PACK, Pack Number DYNJ53588I;   9) CARDIAC CATH PACK, Pack Number DYNJ31733C;   10) CARDIAC CATH PACK, Pack Number DYNJ41315A;   11) CARDIAC CATH PACK-LF, Pack Number DYNJ0380198L;   12) CATH LAB PACK, Pack Number 0M-CP31796Q;   13) CATH LAB PACK-LF, Pack Number DYNJ0194968AG;   14) CATH LAB TRAY, Pack Number 00-401610J;   15) CHRISTUS SR CATH LAB PACK, Pack Number DYNJ60931C;   16) CRMC CATH LAB TRAY JUDKINS-LF, Pack Number DYNJ61088F;   17) CRMC NEURO ENDO HYBRID-LF, Pack Number DYNJ61101D;   18) EP PACK MORNINGSIDE, Pack Number DYNJ69301;   19) FEMORAL TRAY 2, Pack Number DYNJ68812C;   20) INTERVENTIONAL MINOR PACK, Pack Number DYNJ24615D;   21) INTERVENTIONAL PACK, Pack Number DYNJ54253;   22) INTERVENTIONAL RADIOLOGY PK-LF, Pack Number PHS605358025B;   23) MORNINGSIDE CARDIAC CATH, Pack Number DYNJ58339A;   24) OR INTERVENTIONAL PACK, Pack Number DYNJ46934A;   25) PACK,CARDIAC CATH, Pack Number DYNJ65481;   26) PK, RADIOLOGY-SPECIALS, Pack Number DYNJ59628C;   27) PTCA TRAY-LF, Pack Number DYNJ07252V;   28) RADIOLOGY PACK, Pack Number DYNJ45393A;   29) RR-ANGIOGRAPHY DRAPE PACK-LF, Pack Number DYNJ0608549M;   30) SPEC ANGIO PACK (SASJK)642-LF, Pack Number DYNJ47586F;   31) SPECIALS LINE PACK, Pack Number DYNJ69504;   32) TV-CARDIAC CATH PACK-LF, Pack Number DYNJ41564P;   33) TV-CARDIAC CATH PACK-LF, Pack Number DYNJ41564P;   34) UTHET TYLER ELECTROPHYSIOLOGY, Pack Number DYNJ68672C",
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      "name": "MEDLINE INDUSTRIES, LP - Northfield"
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    {
      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-1437-2025/enforcement-record",
      "@type": "schema:Claim",
      "name": "FDA recall Z-1437-2025: MEDLINE INDUSTRIES, LP - Northfield is recalling Medline procedure kits labeled as:    1) ANGIO DRAPE PACK (DRLUL)-LF, Pack Number DYNJ47718D;   2) ANGIO PACK, Pack Number DYNJ69678;   3) ANGIOGRAPHY CV RAD PACK, Pack Number DYNJ64936A;   4) ANGIOGRAPHY DRAPE PACK, Pack Number DYNJ49621C;   5) ANGIOGRAPHY PACK, Pack Number DYNJ61266A;   6) ANGIOGRAPHY PACK-LF, Pack Number DYNJ35916N;   7) ARTERIOGRAM PACK, Pack Number DYNJ34442F;   8) CARDIAC CATH FEMORAL PACK, Pack Number DYNJ53588I;   9) CARDIAC CATH PACK, Pack Number DYNJ31733C;   10) CARDIAC CATH PACK, Pack Number DYNJ41315A;   11) CARDIAC CATH PACK-LF, Pack Number DYNJ0380198L;   12) CATH LAB PACK, Pack Number 0M-CP31796Q;   13) CATH LAB PACK-LF, Pack Number DYNJ0194968AG;   14) CATH LAB TRAY, Pack Number 00-401610J;   15) CHRISTUS SR CATH LAB PACK, Pack Number DYNJ60931C;   16) CRMC CATH LAB TRAY JUDKINS-LF, Pack Number DYNJ61088F;   17) CRMC NEURO ENDO HYBRID-LF, Pack Number DYNJ61101D;   18) EP PACK MORNINGSIDE, Pack Number DYNJ69301;   19) FEMORAL TRAY 2, Pack Number DYNJ68812C;   20) INTERVENTIONAL MINOR PACK, Pack Number DYNJ24615D;   21) INTERVENTIONAL PACK, Pack Number DYNJ54253;   22) INTERVENTIONAL RADIOLOGY PK-LF, Pack Number PHS605358025B;   23) MORNINGSIDE CARDIAC CATH, Pack Number DYNJ58339A;   24) OR INTERVENTIONAL PACK, Pack Number DYNJ46934A;   25) PACK,CARDIAC CATH, Pack Number DYNJ65481;   26) PK, RADIOLOGY-SPECIALS, Pack Number DYNJ59628C;   27) PTCA TRAY-LF, Pack Number DYNJ07252V;   28) RADIOLOGY PACK, Pack Number DYNJ45393A;   29) RR-ANGIOGRAPHY DRAPE PACK-LF, Pack Number DYNJ0608549M;   30) SPEC ANGIO PACK (SASJK)642-LF, Pack Number DYNJ47586F;   31) SPECIALS LINE PACK, Pack Number DYNJ69504;   32) TV-CARDIAC CATH PACK-LF, Pack Number DYNJ41564P;   33) TV-CARDIAC CATH PACK-LF, Pack Number DYNJ41564P;   34) UTHET TYLER ELECTROPHYSIOLOGY, Pack Number DYNJ68672C",
      "text": "The FDA logged enforcement record Z-1437-2025: MEDLINE INDUSTRIES, LP - Northfield is voluntarily recalling Medline procedure kits labeled as:    1) ANGIO DRAPE PACK (DRLUL)-LF, Pack Number DYNJ47718D;   2) ANGIO PACK, Pack Number DYNJ69678;   3) ANGIOGRAPHY CV RAD PACK, Pack Number DYNJ64936A;   4) ANGIOGRAPHY DRAPE PACK, Pack Number DYNJ49621C;   5) ANGIOGRAPHY PACK, Pack Number DYNJ61266A;   6) ANGIOGRAPHY PACK-LF, Pack Number DYNJ35916N;   7) ARTERIOGRAM PACK, Pack Number DYNJ34442F;   8) CARDIAC CATH FEMORAL PACK, Pack Number DYNJ53588I;   9) CARDIAC CATH PACK, Pack Number DYNJ31733C;   10) CARDIAC CATH PACK, Pack Number DYNJ41315A;   11) CARDIAC CATH PACK-LF, Pack Number DYNJ0380198L;   12) CATH LAB PACK, Pack Number 0M-CP31796Q;   13) CATH LAB PACK-LF, Pack Number DYNJ0194968AG;   14) CATH LAB TRAY, Pack Number 00-401610J;   15) CHRISTUS SR CATH LAB PACK, Pack Number DYNJ60931C;   16) CRMC CATH LAB TRAY JUDKINS-LF, Pack Number DYNJ61088F;   17) CRMC NEURO ENDO HYBRID-LF, Pack Number DYNJ61101D;   18) EP PACK MORNINGSIDE, Pack Number DYNJ69301;   19) FEMORAL TRAY 2, Pack Number DYNJ68812C;   20) INTERVENTIONAL MINOR PACK, Pack Number DYNJ24615D;   21) INTERVENTIONAL PACK, Pack Number DYNJ54253;   22) INTERVENTIONAL RADIOLOGY PK-LF, Pack Number PHS605358025B;   23) MORNINGSIDE CARDIAC CATH, Pack Number DYNJ58339A;   24) OR INTERVENTIONAL PACK, Pack Number DYNJ46934A;   25) PACK,CARDIAC CATH, Pack Number DYNJ65481;   26) PK, RADIOLOGY-SPECIALS, Pack Number DYNJ59628C;   27) PTCA TRAY-LF, Pack Number DYNJ07252V;   28) RADIOLOGY PACK, Pack Number DYNJ45393A;   29) RR-ANGIOGRAPHY DRAPE PACK-LF, Pack Number DYNJ0608549M;   30) SPEC ANGIO PACK (SASJK)642-LF, Pack Number DYNJ47586F;   31) SPECIALS LINE PACK, Pack Number DYNJ69504;   32) TV-CARDIAC CATH PACK-LF, Pack Number DYNJ41564P;   33) TV-CARDIAC CATH PACK-LF, Pack Number DYNJ41564P;   34) UTHET TYLER ELECTROPHYSIOLOGY, Pack Number DYNJ68672C — 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 2025-02-11. Affected lots/codes: 1) Pack Number DYNJ47718D:  UDI/DI 10195327528331 (each) 40195327528332 (case), Lot Number 23LME887A;  2) Pack Number DYNJ69678:  UDI/DI 10193489968156 (each) 40193489968157 (case), Lot Number 23EMD520A;  3) Pack Number DYNJ64936A:  UDI/DI 10193489978759 (each) 40193489978750 (case), Lot Number 21LBW389A;  4) Pack Number DYNJ49621C:  UDI/DI 10195327008581 (each) 40195327008582 (case), Lot Number 23LMG954A;  5) Pack Number DYNJ61266A:  UDI/DI 10195327057763 (each) 40195327057764 (case), Lot Number 23GBF536A;  6) Pack Number DYNJ35916N:  UDI/DI 10195327223977 (each) 40195327223978 (case), Lot Number 23EBE626A;  7) Pack Number DYNJ34442F:  UDI/DI 10193489881424 (each) 40193489881425 (case), Lot Number 23LMG342A;  8) Pack Number DYNJ53588I:  UDI/DI 10195327014001 (each) 40195327014002 (case), Lot Number 23EME005A;  9) Pack Number DYNJ31733C:  UDI/DI 10889942875290 (each) 40889942875291 (case), Lot Number 21BBG459B;  10) Pack Number DYNJ41315A:  UDI/DI 10888277907089 (each) 40888277907080 (case), Lot Number 22LBA182A;  11) Pack Number DYNJ0380198L:  UDI/DI 10193489916478 (each) 40193489916479 (case), Lot Number 22GBH915A;  12) Pack Number 0M-CP31796Q:  UDI/DI 10889942756483 (each) 40889942756484 (case), Lot Number 21HBP168A;  13) Pack Number DYNJ0194968AG:  UDI/DI 10195327179557 (each) 40195327179558 (case), Lot Number 24AME980A;  14) Pack Number 00-401610J:  UDI/DI 10889942731640 (each) 40889942731641 (case), Lot Number 23LBL085Z;  15) Pack Number DYNJ60931C:  UDI/DI 10193489952940 (each) 40193489952941 (case), Lot Number 21JMI207A;  16) Pack Number DYNJ61088F:  UDI/DI 10195327451585 (each) 40195327451586 (case), Lot Number 23LMG703A;  17) Pack Number DYNJ61101D:  UDI/DI 10195327451813 (each) 40195327451814 (case), Lot Number 23HME348A;  18) Pack Number DYNJ69301:  UDI/DI 10193489926101 (each) 40193489926102 (case), Lot Number 23CBL353A;  19) Pack Number DYNJ68812C:  UDI/DI 10195327449452 (each) 40195327449453 (case), Lot Number 23KMC169A;  20) Pack Number DYNJ24615D:  UDI/DI 10889942436057 (each) 40889942436058 (case), Lot Number 21JMF491A;  21) Pack Number DYNJ54253:  UDI/DI 10889942474509 (each) 40889942474500 (case), Lot Number 20KBM762A;  22) Pack Number PHS605358025B:  UDI/DI 10193489498998 (each) 40193489498999 (case), Lot Number 23FMD837A;  23) Pack Number DYNJ58339A:  UDI/DI 10193489483147 (each) 40193489483148 (case), Lot Number 21EBP494A;  24) Pack Number DYNJ46934A:  UDI/DI 10888277856998 (each) 40888277856999 (case), Lot Number 23BBR783A;  25) Pack Number DYNJ65481:  UDI/DI 10193489280463 (each) 40193489280464 (case), Lot Number 23IMG363A;  26) Pack Number DYNJ59628C:  UDI/DI 10193489813128 (each) 40193489813129 (case), Lot Number 23LBK499A;  27) Pack Number DYNJ07252V:  UDI/DI 10193489744644 (each) 40193489744645 (case), Lot Number 22HBO256A;  28) Pack Number DYNJ45393A:  UDI/DI 10889942188765 (each) 40889942188766 (case), Lot Number 20FMA718A;  29) Pack Number DYNJ0608549M:  UDI/DI 10195327477387 (each) 40195327477388 (case), Lot Number 23LMD710A;  30) Pack Number DYNJ47586F:  UDI/DI 10195327400156 (each) 40195327400157 (case), Lot Number 23LME689A;  31) Pack Number DYNJ69504:  UDI/DI 10193489950243 (each) 40193489950244 (case), Lot Number 24ABA461Z;  32) Pack Number DYNJ41564P:  UDI/DI 10195327177423 (each) 40195327177424 (case), Lot Number 23HMB245A;  33) Pack Number DYNJ41564P:  UDI/DI 10195327177423 (each) 40195327177424 (case), Lot Number 23HMC543A;  34) Pack Number DYNJ68672C:  UDI/DI 10195327191566 (each) 40195327191567 (case), Lot Number 23BBR790A. A RECORDED FDA enforcement action (occurred=true).",
      "claimType": "official_fact",
      "reviewStatus": "current",
      "commercialInfluence": false,
      "epistemicStatus": {
        "occurred": true,
        "supported": true,
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        "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-1437-2025&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-1437-2025&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-1437-2025/fda-classification",
      "@type": "schema:Claim",
      "name": "FDA classified recall Z-1437-2025 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-1437-2025&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-1437-2025&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-1437-2025/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."
    }
  ],
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      "name": "FDA recall details — Z-1437-2025",
      "numberOfItems": 9,
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          "position": 1,
          "item": {
            "Field": "Recall number",
            "Value": "Z-1437-2025",
            "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": "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"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 7,
          "item": {
            "Field": "Initiated",
            "Value": "2025-02-11",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 8,
          "item": {
            "Field": "Lot/code info",
            "Value": "1) Pack Number DYNJ47718D:  UDI/DI 10195327528331 (each) 40195327528332 (case), Lot Number 23LME887A;  2) Pack Number DYNJ69678:  UDI/DI 10193489968156 (each) 40193489968157 (case), Lot Number 23EMD520A;  3) Pack Number DYNJ64936A:  UDI/DI 10193489978759 (each) 40193489978750 (case), Lot Number 21LBW389A;  4) Pack Number DYNJ49621C:  UDI/DI 10195327008581 (each) 40195327008582 (case), Lot Number 23LMG954A;  5) Pack Number DYNJ61266A:  UDI/DI 10195327057763 (each) 40195327057764 (case), Lot Number 23GBF536A;  6) Pack Number DYNJ35916N:  UDI/DI 10195327223977 (each) 40195327223978 (case), Lot Number 23EBE626A;  7) Pack Number DYNJ34442F:  UDI/DI 10193489881424 (each) 40193489881425 (case), Lot Number 23LMG342A;  8) Pack Number DYNJ53588I:  UDI/DI 10195327014001 (each) 40195327014002 (case), Lot Number 23EME005A;  9) Pack Number DYNJ31733C:  UDI/DI 10889942875290 (each) 40889942875291 (case), Lot Number 21BBG459B;  10) Pack Number DYNJ41315A:  UDI/DI 10888277907089 (each) 40888277907080 (case), Lot Number 22LBA182A;  11) Pack Number DYNJ0380198L:  UDI/DI 10193489916478 (each) 40193489916479 (case), Lot Number 22GBH915A;  12) Pack Number 0M-CP31796Q:  UDI/DI 10889942756483 (each) 40889942756484 (case), Lot Number 21HBP168A;  13) Pack Number DYNJ0194968AG:  UDI/DI 10195327179557 (each) 40195327179558 (case), Lot Number 24AME980A;  14) Pack Number 00-401610J:  UDI/DI 10889942731640 (each) 40889942731641 (case), Lot Number 23LBL085Z;  15) Pack Number DYNJ60931C:  UDI/DI 10193489952940 (each) 40193489952941 (case), Lot Number 21JMI207A;  16) Pack Number DYNJ61088F:  UDI/DI 10195327451585 (each) 40195327451586 (case), Lot Number 23LMG703A;  17) Pack Number DYNJ61101D:  UDI/DI 10195327451813 (each) 40195327451814 (case), Lot Number 23HME348A;  18) Pack Number DYNJ69301:  UDI/DI 10193489926101 (each) 40193489926102 (case), Lot Number 23CBL353A;  19) Pack Number DYNJ68812C:  UDI/DI 10195327449452 (each) 40195327449453 (case), Lot Number 23KMC169A;  20) Pack Number DYNJ24615D:  UDI/DI 10889942436057 (each) 40889942436058 (case), Lot Number 21JMF491A;  21) Pack Number DYNJ54253:  UDI/DI 10889942474509 (each) 40889942474500 (case), Lot Number 20KBM762A;  22) Pack Number PHS605358025B:  UDI/DI 10193489498998 (each) 40193489498999 (case), Lot Number 23FMD837A;  23) Pack Number DYNJ58339A:  UDI/DI 10193489483147 (each) 40193489483148 (case), Lot Number 21EBP494A;  24) Pack Number DYNJ46934A:  UDI/DI 10888277856998 (each) 40888277856999 (case), Lot Number 23BBR783A;  25) Pack Number DYNJ65481:  UDI/DI 10193489280463 (each) 40193489280464 (case), Lot Number 23IMG363A;  26) Pack Number DYNJ59628C:  UDI/DI 10193489813128 (each) 40193489813129 (case), Lot Number 23LBK499A;  27) Pack Number DYNJ07252V:  UDI/DI 10193489744644 (each) 40193489744645 (case), Lot Number 22HBO256A;  28) Pack Number DYNJ45393A:  UDI/DI 10889942188765 (each) 40889942188766 (case), Lot Number 20FMA718A;  29) Pack Number DYNJ0608549M:  UDI/DI 10195327477387 (each) 40195327477388 (case), Lot Number 23LMD710A;  30) Pack Number DYNJ47586F:  UDI/DI 10195327400156 (each) 40195327400157 (case), Lot Number 23LME689A;  31) Pack Number DYNJ69504:  UDI/DI 10193489950243 (each) 40193489950244 (case), Lot Number 24ABA461Z;  32) Pack Number DYNJ41564P:  UDI/DI 10195327177423 (each) 40195327177424 (case), Lot Number 23HMB245A;  33) Pack Number DYNJ41564P:  UDI/DI 10195327177423 (each) 40195327177424 (case), Lot Number 23HMC543A;  34) Pack Number DYNJ68672C:  UDI/DI 10195327191566 (each) 40195327191567 (case), Lot Number 23BBR790A",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 9,
          "item": {
            "Field": "Distribution pattern",
            "Value": "Worldwide distribution - US Nationwide and the country of Canada.",
            "Status": "recorded"
          }
        }
      ]
    }
  ]
}