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  "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-2747-2024.jsonld",
  "@type": "schema:Dataset",
  "name": "Medline procedural kits labeled as:    1) TYMPANOPLASTY , Pack Number CDS980203S;   2) MAJOR EAR , Pack Number CDS982016T;   3) MAJOR EAR PACK, Pack Number CMPJ01846O;   4) EAR PACK, Pack Number CMPJ05884J;   5) MZ EAR PACK , Pack Number CMPJ09860D;   6) KIT MAJOR EAR CHRG, Pack Number CMPJ09914C;   7) ENT PACK, Pack Number CMPJ13389A;   8) ENT PACK, Pack Number CMPJ13389B;   9) ENT PACK, Pack Number CMPJ13389C;   10) DR LIN EAR PACK , Pack Number CMPJ13509 ;   11) TYMPANOPLASTY PACK, Pack Number CMPJ21114O;   12) EAR PACK-LF , Pack Number DYNJ0425965G  ;   13) EAR PACK-LF , Pack Number DYNJ0774664K  ;   14) HL EAR PACK , Pack Number DYNJ40560B;   15) HL EAR PACK , Pack Number DYNJ40560BH;   16) EAR PACK, Pack Number DYNJ44134C;   17) EAR PACK, Pack Number DYNJ44134D;   18) EAR PACK, Pack Number DYNJ44134F;   19) MINOR ENT PACK, Pack Number DYNJ45577A;   20) ENT PACK, Pack Number DYNJ48595 ;   21) MH NASAL, Pack Number DYNJ49888I;   22) MH NASAL, Pack Number DYNJ49888J;   23) MIDDLE EAR OR , Pack Number DYNJ52583G;   24) MIDDLE EAR OR , Pack Number DYNJ52583J;   25) MIDDLE EAR OR , Pack Number DYNJ52583L;   26) ***, Pack Number DYNJ52583M;   27) GLENNON HEAD AND NECK PACK-LF , Pack Number DYNJ57200A;   28) MIDDLE EAR PACK , Pack Number DYNJ65935A;   29) ENT PACK, Pack Number DYNJ66039B;   30) FACIAL PACK , Pack Number DYNJ82177B;   31) FACIAL PACK , Pack Number DYNJ82177BH;   32) EAR CUSTOM PACK , Pack Number DYNJ82564 ;   33) ***, Pack Number DYNJ86113 ;   34) EAR , Pack Number DYNJ901779J;   35) MZ EAR CDS, Pack Number DYNJ905642D;   36) PACK MAJOR EAR CHRG , Pack Number DYNJ905694C;   37) ENT , Pack Number DYNJ909128A;   38) ENT , Pack Number DYNJ909128C;   39) ENT , Pack Number DYNJ909128D;   40) ***, Pack Number DYNJ909128D;   41) DR LIN EAR, Pack Number DYNJ909251;   42) T AND A , Pack Number DYNJ909941;   43) ***, Pack Number DYNJ909941",
  "description": "FDA recall Z-2747-2024 — MEDLINE INDUSTRIES, LP - Northfield is recalling Medline procedural kits labeled as:    1) TYMPANOPLASTY , Pack Number CDS980203S;   2) MAJOR EAR , Pack Number CDS982016T;   3) MAJOR EAR PACK, Pack Number CMPJ01846O;   4) EAR PACK, Pack Number CMPJ05884J;   5) MZ EAR PACK , Pack Number CMPJ09860D;   6) KIT MAJOR EAR CHRG, Pack Number CMPJ09914C;   7) ENT PACK, Pack Number CMPJ13389A;   8) ENT PACK, Pack Number CMPJ13389B;   9) ENT PACK, Pack Number CMPJ13389C;   10) DR LIN EAR PACK , Pack Number CMPJ13509 ;   11) TYMPANOPLASTY PACK, Pack Number CMPJ21114O;   12) EAR PACK-LF , Pack Number DYNJ0425965G  ;   13) EAR PACK-LF , Pack Number DYNJ0774664K  ;   14) HL EAR PACK , Pack Number DYNJ40560B;   15) HL EAR PACK , Pack Number DYNJ40560BH;   16) EAR PACK, Pack Number DYNJ44134C;   17) EAR PACK, Pack Number DYNJ44134D;   18) EAR PACK, Pack Number DYNJ44134F;   19) MINOR ENT PACK, Pack Number DYNJ45577A;   20) ENT PACK, Pack Number DYNJ48595 ;   21) MH NASAL, Pack Number DYNJ49888I;   22) MH NASAL, Pack Number DYNJ49888J;   23) MIDDLE EAR OR , Pack Number DYNJ52583G;   24) MIDDLE EAR OR , Pack Number DYNJ52583J;   25) MIDDLE EAR OR , Pack Number DYNJ52583L;   26) ***, Pack Number DYNJ52583M;   27) GLENNON HEAD AND NECK PACK-LF , Pack Number DYNJ57200A;   28) MIDDLE EAR PACK , Pack Number DYNJ65935A;   29) ENT PACK, Pack Number DYNJ66039B;   30) FACIAL PACK , Pack Number DYNJ82177B;   31) FACIAL PACK , Pack Number DYNJ82177BH;   32) EAR CUSTOM PACK , Pack Number DYNJ82564 ;   33) ***, Pack Number DYNJ86113 ;   34) EAR , Pack Number DYNJ901779J;   35) MZ EAR CDS, Pack Number DYNJ905642D;   36) PACK MAJOR EAR CHRG , Pack Number DYNJ905694C;   37) ENT , Pack Number DYNJ909128A;   38) ENT , Pack Number DYNJ909128C;   39) ENT , Pack Number DYNJ909128D;   40) ***, Pack Number DYNJ909128D;   41) DR LIN EAR, Pack Number DYNJ909251;   42) T AND A , Pack Number DYNJ909941;   43) ***, Pack Number DYNJ909941 (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 procedural kits labeled as:    1) TYMPANOPLASTY , Pack Number CDS980203S;   2) MAJOR EAR , Pack Number CDS982016T;   3) MAJOR EAR PACK, Pack Number CMPJ01846O;   4) EAR PACK, Pack Number CMPJ05884J;   5) MZ EAR PACK , Pack Number CMPJ09860D;   6) KIT MAJOR EAR CHRG, Pack Number CMPJ09914C;   7) ENT PACK, Pack Number CMPJ13389A;   8) ENT PACK, Pack Number CMPJ13389B;   9) ENT PACK, Pack Number CMPJ13389C;   10) DR LIN EAR PACK , Pack Number CMPJ13509 ;   11) TYMPANOPLASTY PACK, Pack Number CMPJ21114O;   12) EAR PACK-LF , Pack Number DYNJ0425965G  ;   13) EAR PACK-LF , Pack Number DYNJ0774664K  ;   14) HL EAR PACK , Pack Number DYNJ40560B;   15) HL EAR PACK , Pack Number DYNJ40560BH;   16) EAR PACK, Pack Number DYNJ44134C;   17) EAR PACK, Pack Number DYNJ44134D;   18) EAR PACK, Pack Number DYNJ44134F;   19) MINOR ENT PACK, Pack Number DYNJ45577A;   20) ENT PACK, Pack Number DYNJ48595 ;   21) MH NASAL, Pack Number DYNJ49888I;   22) MH NASAL, Pack Number DYNJ49888J;   23) MIDDLE EAR OR , Pack Number DYNJ52583G;   24) MIDDLE EAR OR , Pack Number DYNJ52583J;   25) MIDDLE EAR OR , Pack Number DYNJ52583L;   26) ***, Pack Number DYNJ52583M;   27) GLENNON HEAD AND NECK PACK-LF , Pack Number DYNJ57200A;   28) MIDDLE EAR PACK , Pack Number DYNJ65935A;   29) ENT PACK, Pack Number DYNJ66039B;   30) FACIAL PACK , Pack Number DYNJ82177B;   31) FACIAL PACK , Pack Number DYNJ82177BH;   32) EAR CUSTOM PACK , Pack Number DYNJ82564 ;   33) ***, Pack Number DYNJ86113 ;   34) EAR , Pack Number DYNJ901779J;   35) MZ EAR CDS, Pack Number DYNJ905642D;   36) PACK MAJOR EAR CHRG , Pack Number DYNJ905694C;   37) ENT , Pack Number DYNJ909128A;   38) ENT , Pack Number DYNJ909128C;   39) ENT , Pack Number DYNJ909128D;   40) ***, Pack Number DYNJ909128D;   41) DR LIN EAR, Pack Number DYNJ909251;   42) T AND A , Pack Number DYNJ909941;   43) ***, Pack Number DYNJ909941",
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    {
      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-2747-2024/enforcement-record",
      "@type": "schema:Claim",
      "name": "FDA recall Z-2747-2024: MEDLINE INDUSTRIES, LP - Northfield is recalling Medline procedural kits labeled as:    1) TYMPANOPLASTY , Pack Number CDS980203S;   2) MAJOR EAR , Pack Number CDS982016T;   3) MAJOR EAR PACK, Pack Number CMPJ01846O;   4) EAR PACK, Pack Number CMPJ05884J;   5) MZ EAR PACK , Pack Number CMPJ09860D;   6) KIT MAJOR EAR CHRG, Pack Number CMPJ09914C;   7) ENT PACK, Pack Number CMPJ13389A;   8) ENT PACK, Pack Number CMPJ13389B;   9) ENT PACK, Pack Number CMPJ13389C;   10) DR LIN EAR PACK , Pack Number CMPJ13509 ;   11) TYMPANOPLASTY PACK, Pack Number CMPJ21114O;   12) EAR PACK-LF , Pack Number DYNJ0425965G  ;   13) EAR PACK-LF , Pack Number DYNJ0774664K  ;   14) HL EAR PACK , Pack Number DYNJ40560B;   15) HL EAR PACK , Pack Number DYNJ40560BH;   16) EAR PACK, Pack Number DYNJ44134C;   17) EAR PACK, Pack Number DYNJ44134D;   18) EAR PACK, Pack Number DYNJ44134F;   19) MINOR ENT PACK, Pack Number DYNJ45577A;   20) ENT PACK, Pack Number DYNJ48595 ;   21) MH NASAL, Pack Number DYNJ49888I;   22) MH NASAL, Pack Number DYNJ49888J;   23) MIDDLE EAR OR , Pack Number DYNJ52583G;   24) MIDDLE EAR OR , Pack Number DYNJ52583J;   25) MIDDLE EAR OR , Pack Number DYNJ52583L;   26) ***, Pack Number DYNJ52583M;   27) GLENNON HEAD AND NECK PACK-LF , Pack Number DYNJ57200A;   28) MIDDLE EAR PACK , Pack Number DYNJ65935A;   29) ENT PACK, Pack Number DYNJ66039B;   30) FACIAL PACK , Pack Number DYNJ82177B;   31) FACIAL PACK , Pack Number DYNJ82177BH;   32) EAR CUSTOM PACK , Pack Number DYNJ82564 ;   33) ***, Pack Number DYNJ86113 ;   34) EAR , Pack Number DYNJ901779J;   35) MZ EAR CDS, Pack Number DYNJ905642D;   36) PACK MAJOR EAR CHRG , Pack Number DYNJ905694C;   37) ENT , Pack Number DYNJ909128A;   38) ENT , Pack Number DYNJ909128C;   39) ENT , Pack Number DYNJ909128D;   40) ***, Pack Number DYNJ909128D;   41) DR LIN EAR, Pack Number DYNJ909251;   42) T AND A , Pack Number DYNJ909941;   43) ***, Pack Number DYNJ909941",
      "text": "The FDA logged enforcement record Z-2747-2024: MEDLINE INDUSTRIES, LP - Northfield is voluntarily recalling Medline procedural kits labeled as:    1) TYMPANOPLASTY , Pack Number CDS980203S;   2) MAJOR EAR , Pack Number CDS982016T;   3) MAJOR EAR PACK, Pack Number CMPJ01846O;   4) EAR PACK, Pack Number CMPJ05884J;   5) MZ EAR PACK , Pack Number CMPJ09860D;   6) KIT MAJOR EAR CHRG, Pack Number CMPJ09914C;   7) ENT PACK, Pack Number CMPJ13389A;   8) ENT PACK, Pack Number CMPJ13389B;   9) ENT PACK, Pack Number CMPJ13389C;   10) DR LIN EAR PACK , Pack Number CMPJ13509 ;   11) TYMPANOPLASTY PACK, Pack Number CMPJ21114O;   12) EAR PACK-LF , Pack Number DYNJ0425965G  ;   13) EAR PACK-LF , Pack Number DYNJ0774664K  ;   14) HL EAR PACK , Pack Number DYNJ40560B;   15) HL EAR PACK , Pack Number DYNJ40560BH;   16) EAR PACK, Pack Number DYNJ44134C;   17) EAR PACK, Pack Number DYNJ44134D;   18) EAR PACK, Pack Number DYNJ44134F;   19) MINOR ENT PACK, Pack Number DYNJ45577A;   20) ENT PACK, Pack Number DYNJ48595 ;   21) MH NASAL, Pack Number DYNJ49888I;   22) MH NASAL, Pack Number DYNJ49888J;   23) MIDDLE EAR OR , Pack Number DYNJ52583G;   24) MIDDLE EAR OR , Pack Number DYNJ52583J;   25) MIDDLE EAR OR , Pack Number DYNJ52583L;   26) ***, Pack Number DYNJ52583M;   27) GLENNON HEAD AND NECK PACK-LF , Pack Number DYNJ57200A;   28) MIDDLE EAR PACK , Pack Number DYNJ65935A;   29) ENT PACK, Pack Number DYNJ66039B;   30) FACIAL PACK , Pack Number DYNJ82177B;   31) FACIAL PACK , Pack Number DYNJ82177BH;   32) EAR CUSTOM PACK , Pack Number DYNJ82564 ;   33) ***, Pack Number DYNJ86113 ;   34) EAR , Pack Number DYNJ901779J;   35) MZ EAR CDS, Pack Number DYNJ905642D;   36) PACK MAJOR EAR CHRG , Pack Number DYNJ905694C;   37) ENT , Pack Number DYNJ909128A;   38) ENT , Pack Number DYNJ909128C;   39) ENT , Pack Number DYNJ909128D;   40) ***, Pack Number DYNJ909128D;   41) DR LIN EAR, Pack Number DYNJ909251;   42) T AND A , Pack Number DYNJ909941;   43) ***, Pack Number DYNJ909941 — 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: CDS980203S, Lot Numbers:23DBT154;  CDS980203S, Lot Numbers:23HBT797;  CDS980203S, Lot Numbers:23JBM122;  CDS980203S, Lot Numbers:23LBC884;  CDS980203S, Lot Numbers:21CBW683;  CDS982016T, Lot Numbers:22GBM951;  CDS982016T, Lot Numbers:22GBO165;  CDS982016T, Lot Numbers:22HBS644;  CMPJ01846O, Lot Numbers:21LBQ988;  CMPJ01846O, Lot Numbers:22FBV101;  CMPJ05884J, Lot Numbers:21KBO037;  CMPJ05884J, Lot Numbers:21KBU691;  CMPJ05884J, Lot Numbers:21LBH778;  CMPJ05884J, Lot Numbers:22IBG052;  CMPJ05884J, Lot Numbers:22JBN865;  CMPJ09860D, Lot Numbers:23KMB793;  CMPJ09914C, Lot Numbers:23IDA209;  CMPJ13389A, Lot Numbers:23CBL552;  CMPJ13389B, Lot Numbers:23IBC818;  CMPJ13389C, Lot Numbers:23KBU012;  CMPJ13389C, Lot Numbers:23LBF106;  CMPJ13389C, Lot Numbers:24ABD504;  CMPJ13389C, Lot Numbers:24ABY610;  CMPJ13389C, Lot Numbers:24BBV889;  CMPJ13509, Lot Numbers:23IBF142;  CMPJ21114O, Lot Numbers:23BBQ474;  CMPJ21114O, Lot Numbers:23HBG033;  CMPJ21114O, Lot Numbers:23IBV766;  CMPJ21114O, Lot Numbers:23JBM292;  CMPJ21114O, Lot Numbers:23KBK531;  CMPJ21114O, Lot Numbers:21BBJ985;  DYNJ0425965G, Lot Numbers:23GMH984;  DYNJ0774664K, Lot Numbers:23HBP871;  DYNJ40560B, Lot Numbers:23HBF219;  DYNJ40560BH , Lot Numbers:23HBF219;  DYNJ44134C, Lot Numbers:22JBQ075;  DYNJ44134D, Lot Numbers:23BBK410;  DYNJ44134D, Lot Numbers:23CBS145;  DYNJ44134F, Lot Numbers:23EBC602;  DYNJ44134F, Lot Numbers:23GBV482;  DYNJ44134F, Lot Numbers:23JBP398;  DYNJ44134F, Lot Numbers:23KBN024;  DYNJ44134F, Lot Numbers:24ABC027;  DYNJ45577A, Lot Numbers:21KBL221;  DYNJ45577A, Lot Numbers:21KBT524;  DYNJ48595, Lot Numbers:24BBO457;  DYNJ49888I, Lot Numbers:22AMG372;  DYNJ49888I, Lot Numbers:22KMD386;  DYNJ49888J, Lot Numbers:24AMG698;  DYNJ52583G, Lot Numbers:21HBC324;  DYNJ52583G, Lot Numbers:21KBM269;  DYNJ52583J, Lot Numbers:21LBN305;  DYNJ52583L, Lot Numbers:22DBB163;  DYNJ52583L, Lot Numbers:22FBF207;  DYNJ52583L, Lot Numbers:22HMF439;  DYNJ52583L, Lot Numbers:22JMC614;  DYNJ52583L, Lot Numbers:23JMF994;  DYNJ52583M, Lot Numbers:24CMF962;  DYNJ57200A, Lot Numbers:23HBN488;  DYNJ65935A, Lot Numbers:23HBR355;  DYNJ65935A, Lot Numbers:23HBT376;  DYNJ66039B, Lot Numbers:23GBQ016;  DYNJ82177B, Lot Numbers:23KMB826;  DYNJ82177BH , Lot Numbers:23KMB826;  DYNJ82564, Lot Numbers:23GBV431;  DYNJ86113, Lot Numbers:24CBE092;  DYNJ901779J , Lot Numbers:21KBY716;  DYNJ901779J , Lot Numbers:21LBS995;  DYNJ901779J , Lot Numbers:21LBV102;  DYNJ901779J , Lot Numbers:22IBS613;  DYNJ901779J , Lot Numbers:22JBY312;  DYNJ901779J , Lot Numbers:22JBY313;  DYNJ901779J , Lot Numbers:23BBB017;  DYNJ905642D , Lot Numbers:23KMH482;  DYNJ905694C , Lot Numbers:23IDB849;  DYNJ909128A , Lot Numbers:23DBD851;  DYNJ909128C , Lot Numbers:23JBO251;  DYNJ909128D , Lot Numbers:23LBM416;  DYNJ909128D , Lot Numbers:23LBQ695;  DYNJ909128D , Lot Numbers:24ABR742;  DYNJ909128D , Lot Numbers:24BBM816;  DYNJ909128D , Lot Numbers:24CBK211;  DYNJ909251, Lot Numbers:23IBT842;  DYNJ909251, Lot Numbers:23IBT854;  DYNJ909251, Lot Numbers:23IBV449;  DYNJ909251, Lot Numbers:23JBT806;  DYNJ909941, Lot Numbers:23JBH984;  DYNJ909941, Lot Numbers:24ABD605;  DYNJ909941, Lot Numbers:24ABD695;  DYNJ909941, Lot Numbers:24ABT569;  DYNJ909941, Lot Numbers:24CBK472. 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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        "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-2747-2024&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-2747-2024&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-2747-2024/fda-classification",
      "@type": "schema:Claim",
      "name": "FDA classified recall Z-2747-2024 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-2747-2024&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-2747-2024&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-2747-2024/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."
    }
  ],
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      "name": "FDA recall details — Z-2747-2024",
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            "Field": "Recall number",
            "Value": "Z-2747-2024",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 2,
          "item": {
            "Field": "Product type",
            "Value": "Devices",
            "Status": "recorded"
          }
        },
        {
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          "position": 3,
          "item": {
            "Field": "Classification",
            "Value": "Class II",
            "Status": "determination"
          }
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          "position": 4,
          "item": {
            "Field": "Status",
            "Value": "Ongoing — the recall is still being carried out.",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 5,
          "item": {
            "Field": "Recalling firm",
            "Value": "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": "2024-04-08",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 8,
          "item": {
            "Field": "Lot/code info",
            "Value": "CDS980203S, Lot Numbers:23DBT154;  CDS980203S, Lot Numbers:23HBT797;  CDS980203S, Lot Numbers:23JBM122;  CDS980203S, Lot Numbers:23LBC884;  CDS980203S, Lot Numbers:21CBW683;  CDS982016T, Lot Numbers:22GBM951;  CDS982016T, Lot Numbers:22GBO165;  CDS982016T, Lot Numbers:22HBS644;  CMPJ01846O, Lot Numbers:21LBQ988;  CMPJ01846O, Lot Numbers:22FBV101;  CMPJ05884J, Lot Numbers:21KBO037;  CMPJ05884J, Lot Numbers:21KBU691;  CMPJ05884J, Lot Numbers:21LBH778;  CMPJ05884J, Lot Numbers:22IBG052;  CMPJ05884J, Lot Numbers:22JBN865;  CMPJ09860D, Lot Numbers:23KMB793;  CMPJ09914C, Lot Numbers:23IDA209;  CMPJ13389A, Lot Numbers:23CBL552;  CMPJ13389B, Lot Numbers:23IBC818;  CMPJ13389C, Lot Numbers:23KBU012;  CMPJ13389C, Lot Numbers:23LBF106;  CMPJ13389C, Lot Numbers:24ABD504;  CMPJ13389C, Lot Numbers:24ABY610;  CMPJ13389C, Lot Numbers:24BBV889;  CMPJ13509, Lot Numbers:23IBF142;  CMPJ21114O, Lot Numbers:23BBQ474;  CMPJ21114O, Lot Numbers:23HBG033;  CMPJ21114O, Lot Numbers:23IBV766;  CMPJ21114O, Lot Numbers:23JBM292;  CMPJ21114O, Lot Numbers:23KBK531;  CMPJ21114O, Lot Numbers:21BBJ985;  DYNJ0425965G, Lot Numbers:23GMH984;  DYNJ0774664K, Lot Numbers:23HBP871;  DYNJ40560B, Lot Numbers:23HBF219;  DYNJ40560BH , Lot Numbers:23HBF219;  DYNJ44134C, Lot Numbers:22JBQ075;  DYNJ44134D, Lot Numbers:23BBK410;  DYNJ44134D, Lot Numbers:23CBS145;  DYNJ44134F, Lot Numbers:23EBC602;  DYNJ44134F, Lot Numbers:23GBV482;  DYNJ44134F, Lot Numbers:23JBP398;  DYNJ44134F, Lot Numbers:23KBN024;  DYNJ44134F, Lot Numbers:24ABC027;  DYNJ45577A, Lot Numbers:21KBL221;  DYNJ45577A, Lot Numbers:21KBT524;  DYNJ48595, Lot Numbers:24BBO457;  DYNJ49888I, Lot Numbers:22AMG372;  DYNJ49888I, Lot Numbers:22KMD386;  DYNJ49888J, Lot Numbers:24AMG698;  DYNJ52583G, Lot Numbers:21HBC324;  DYNJ52583G, Lot Numbers:21KBM269;  DYNJ52583J, Lot Numbers:21LBN305;  DYNJ52583L, Lot Numbers:22DBB163;  DYNJ52583L, Lot Numbers:22FBF207;  DYNJ52583L, Lot Numbers:22HMF439;  DYNJ52583L, Lot Numbers:22JMC614;  DYNJ52583L, Lot Numbers:23JMF994;  DYNJ52583M, Lot Numbers:24CMF962;  DYNJ57200A, Lot Numbers:23HBN488;  DYNJ65935A, Lot Numbers:23HBR355;  DYNJ65935A, Lot Numbers:23HBT376;  DYNJ66039B, Lot Numbers:23GBQ016;  DYNJ82177B, Lot Numbers:23KMB826;  DYNJ82177BH , Lot Numbers:23KMB826;  DYNJ82564, Lot Numbers:23GBV431;  DYNJ86113, Lot Numbers:24CBE092;  DYNJ901779J , Lot Numbers:21KBY716;  DYNJ901779J , Lot Numbers:21LBS995;  DYNJ901779J , Lot Numbers:21LBV102;  DYNJ901779J , Lot Numbers:22IBS613;  DYNJ901779J , Lot Numbers:22JBY312;  DYNJ901779J , Lot Numbers:22JBY313;  DYNJ901779J , Lot Numbers:23BBB017;  DYNJ905642D , Lot Numbers:23KMH482;  DYNJ905694C , Lot Numbers:23IDB849;  DYNJ909128A , Lot Numbers:23DBD851;  DYNJ909128C , Lot Numbers:23JBO251;  DYNJ909128D , Lot Numbers:23LBM416;  DYNJ909128D , Lot Numbers:23LBQ695;  DYNJ909128D , Lot Numbers:24ABR742;  DYNJ909128D , Lot Numbers:24BBM816;  DYNJ909128D , Lot Numbers:24CBK211;  DYNJ909251, Lot Numbers:23IBT842;  DYNJ909251, Lot Numbers:23IBT854;  DYNJ909251, Lot Numbers:23IBV449;  DYNJ909251, Lot Numbers:23JBT806;  DYNJ909941, Lot Numbers:23JBH984;  DYNJ909941, Lot Numbers:24ABD605;  DYNJ909941, Lot Numbers:24ABD695;  DYNJ909941, Lot Numbers:24ABT569;  DYNJ909941, Lot Numbers:24CBK472",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 9,
          "item": {
            "Field": "Distribution pattern",
            "Value": "Worldwide",
            "Status": "recorded"
          }
        }
      ]
    }
  ]
}