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  "name": "Medline Convenience kits used for various procedures:  1) OCULOPLASTIC PICK PACK, Model Number: DYNJ43914B;   2) PLASTIC PACK, Model Number: DYNJ65109;   3) PLASTIC PROCEDURE PACK, Model Number: DYNJ34160D;   4) MINOR BREAST SJHC-LF, Model Number: DYNJ84991;   5) PLASTIC PACK, Model Number: DYNJ66056;   6) MUSCLE PLASTIC PACK, Model Number: DYNJ66212A;   7) MINOR PLASTIC PACK, Model Number: DYNJ37231B;   8) GENERAL BREAST GRH-LF, Model Number: DYNJ52658D;   9) GENERAL BREAST GRH-LF, Model Number: DYNJ52658D;   10) FACE PACK, Model Number: DYNJ37316D;   11) PLASTIC PACK-LF, Model Number: DYNJ57440D;   12) MINOR BREAST SJHC-LF, Model Number: DYNJ84991;   13) MINOR PLASTIC PACK, Model Number: DYNJ37231B;   14) SATELLITE MINOR PLASTIC PACK, Model Number: DYNJ63696;   15) FACIAL/EYE PACK, Model Number: DYNJ68328;   16) BREAST PACK, Model Number: DYNJ63753;   17) BREAST PACK, Model Number: DYNJ63753;   18) TUMMY PACK, Model Number: DYNJ64886A;   19) PLASTIC TORSO PK TEGH-LF, Model Number: DYNJ46737A;   20) PLASTIC BREAST PACK, Model Number: DYNJ40620F;   21) PLASTIC ENT PACK, Model Number: DYNJ64712B;   22) PLASTIC SURGERY SERV-DR GARAZO, Model Number: DYNJ34199A;   23) OCULOPLASTIC PICK PACK, Model Number: DYNJ43914B;   24) OCULAR PLASTICS, Model Number: DYNJ55985D;   25) TUMMY PACK, Model Number: DYNJ64886A;   26) MUSCLE PLASTIC PACK, Model Number: DYNJ66212A;   27) ZURI BREAST PACK, Model Number: DYNJ67772A;   28) PLASTIC TORSO PK TEGH-LF, Model Number: DYNJ46737A;   29) TUMMY PACK, Model Number: DYNJ64886A;   30) OCCULAR PLASTIC PACK, Model Number: DYNJ35741D;   31) FACELIFT PACK, Model Number: DYNJ38907;   32) BREAST PACK, Model Number: DYNJ67882;   33) KDOP PLASTIC PACK, Model Number: DYNJ37142D",
  "description": "FDA recall Z-1600-2025 — MEDLINE INDUSTRIES, LP - Northfield is recalling Medline Convenience kits used for various procedures:  1) OCULOPLASTIC PICK PACK, Model Number: DYNJ43914B;   2) PLASTIC PACK, Model Number: DYNJ65109;   3) PLASTIC PROCEDURE PACK, Model Number: DYNJ34160D;   4) MINOR BREAST SJHC-LF, Model Number: DYNJ84991;   5) PLASTIC PACK, Model Number: DYNJ66056;   6) MUSCLE PLASTIC PACK, Model Number: DYNJ66212A;   7) MINOR PLASTIC PACK, Model Number: DYNJ37231B;   8) GENERAL BREAST GRH-LF, Model Number: DYNJ52658D;   9) GENERAL BREAST GRH-LF, Model Number: DYNJ52658D;   10) FACE PACK, Model Number: DYNJ37316D;   11) PLASTIC PACK-LF, Model Number: DYNJ57440D;   12) MINOR BREAST SJHC-LF, Model Number: DYNJ84991;   13) MINOR PLASTIC PACK, Model Number: DYNJ37231B;   14) SATELLITE MINOR PLASTIC PACK, Model Number: DYNJ63696;   15) FACIAL/EYE PACK, Model Number: DYNJ68328;   16) BREAST PACK, Model Number: DYNJ63753;   17) BREAST PACK, Model Number: DYNJ63753;   18) TUMMY PACK, Model Number: DYNJ64886A;   19) PLASTIC TORSO PK TEGH-LF, Model Number: DYNJ46737A;   20) PLASTIC BREAST PACK, Model Number: DYNJ40620F;   21) PLASTIC ENT PACK, Model Number: DYNJ64712B;   22) PLASTIC SURGERY SERV-DR GARAZO, Model Number: DYNJ34199A;   23) OCULOPLASTIC PICK PACK, Model Number: DYNJ43914B;   24) OCULAR PLASTICS, Model Number: DYNJ55985D;   25) TUMMY PACK, Model Number: DYNJ64886A;   26) MUSCLE PLASTIC PACK, Model Number: DYNJ66212A;   27) ZURI BREAST PACK, Model Number: DYNJ67772A;   28) PLASTIC TORSO PK TEGH-LF, Model Number: DYNJ46737A;   29) TUMMY PACK, Model Number: DYNJ64886A;   30) OCCULAR PLASTIC PACK, Model Number: DYNJ35741D;   31) FACELIFT PACK, Model Number: DYNJ38907;   32) BREAST PACK, Model Number: DYNJ67882;   33) KDOP PLASTIC PACK, Model Number: DYNJ37142D (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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    "@type": "schema:MedicalDevice",
    "name": "Medline Convenience kits used for various procedures:  1) OCULOPLASTIC PICK PACK, Model Number: DYNJ43914B;   2) PLASTIC PACK, Model Number: DYNJ65109;   3) PLASTIC PROCEDURE PACK, Model Number: DYNJ34160D;   4) MINOR BREAST SJHC-LF, Model Number: DYNJ84991;   5) PLASTIC PACK, Model Number: DYNJ66056;   6) MUSCLE PLASTIC PACK, Model Number: DYNJ66212A;   7) MINOR PLASTIC PACK, Model Number: DYNJ37231B;   8) GENERAL BREAST GRH-LF, Model Number: DYNJ52658D;   9) GENERAL BREAST GRH-LF, Model Number: DYNJ52658D;   10) FACE PACK, Model Number: DYNJ37316D;   11) PLASTIC PACK-LF, Model Number: DYNJ57440D;   12) MINOR BREAST SJHC-LF, Model Number: DYNJ84991;   13) MINOR PLASTIC PACK, Model Number: DYNJ37231B;   14) SATELLITE MINOR PLASTIC PACK, Model Number: DYNJ63696;   15) FACIAL/EYE PACK, Model Number: DYNJ68328;   16) BREAST PACK, Model Number: DYNJ63753;   17) BREAST PACK, Model Number: DYNJ63753;   18) TUMMY PACK, Model Number: DYNJ64886A;   19) PLASTIC TORSO PK TEGH-LF, Model Number: DYNJ46737A;   20) PLASTIC BREAST PACK, Model Number: DYNJ40620F;   21) PLASTIC ENT PACK, Model Number: DYNJ64712B;   22) PLASTIC SURGERY SERV-DR GARAZO, Model Number: DYNJ34199A;   23) OCULOPLASTIC PICK PACK, Model Number: DYNJ43914B;   24) OCULAR PLASTICS, Model Number: DYNJ55985D;   25) TUMMY PACK, Model Number: DYNJ64886A;   26) MUSCLE PLASTIC PACK, Model Number: DYNJ66212A;   27) ZURI BREAST PACK, Model Number: DYNJ67772A;   28) PLASTIC TORSO PK TEGH-LF, Model Number: DYNJ46737A;   29) TUMMY PACK, Model Number: DYNJ64886A;   30) OCCULAR PLASTIC PACK, Model Number: DYNJ35741D;   31) FACELIFT PACK, Model Number: DYNJ38907;   32) BREAST PACK, Model Number: DYNJ67882;   33) KDOP PLASTIC PACK, Model Number: DYNJ37142D",
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      "@type": "schema:Claim",
      "name": "FDA recall Z-1600-2025: MEDLINE INDUSTRIES, LP - Northfield is recalling Medline Convenience kits used for various procedures:  1) OCULOPLASTIC PICK PACK, Model Number: DYNJ43914B;   2) PLASTIC PACK, Model Number: DYNJ65109;   3) PLASTIC PROCEDURE PACK, Model Number: DYNJ34160D;   4) MINOR BREAST SJHC-LF, Model Number: DYNJ84991;   5) PLASTIC PACK, Model Number: DYNJ66056;   6) MUSCLE PLASTIC PACK, Model Number: DYNJ66212A;   7) MINOR PLASTIC PACK, Model Number: DYNJ37231B;   8) GENERAL BREAST GRH-LF, Model Number: DYNJ52658D;   9) GENERAL BREAST GRH-LF, Model Number: DYNJ52658D;   10) FACE PACK, Model Number: DYNJ37316D;   11) PLASTIC PACK-LF, Model Number: DYNJ57440D;   12) MINOR BREAST SJHC-LF, Model Number: DYNJ84991;   13) MINOR PLASTIC PACK, Model Number: DYNJ37231B;   14) SATELLITE MINOR PLASTIC PACK, Model Number: DYNJ63696;   15) FACIAL/EYE PACK, Model Number: DYNJ68328;   16) BREAST PACK, Model Number: DYNJ63753;   17) BREAST PACK, Model Number: DYNJ63753;   18) TUMMY PACK, Model Number: DYNJ64886A;   19) PLASTIC TORSO PK TEGH-LF, Model Number: DYNJ46737A;   20) PLASTIC BREAST PACK, Model Number: DYNJ40620F;   21) PLASTIC ENT PACK, Model Number: DYNJ64712B;   22) PLASTIC SURGERY SERV-DR GARAZO, Model Number: DYNJ34199A;   23) OCULOPLASTIC PICK PACK, Model Number: DYNJ43914B;   24) OCULAR PLASTICS, Model Number: DYNJ55985D;   25) TUMMY PACK, Model Number: DYNJ64886A;   26) MUSCLE PLASTIC PACK, Model Number: DYNJ66212A;   27) ZURI BREAST PACK, Model Number: DYNJ67772A;   28) PLASTIC TORSO PK TEGH-LF, Model Number: DYNJ46737A;   29) TUMMY PACK, Model Number: DYNJ64886A;   30) OCCULAR PLASTIC PACK, Model Number: DYNJ35741D;   31) FACELIFT PACK, Model Number: DYNJ38907;   32) BREAST PACK, Model Number: DYNJ67882;   33) KDOP PLASTIC PACK, Model Number: DYNJ37142D",
      "text": "The FDA logged enforcement record Z-1600-2025: MEDLINE INDUSTRIES, LP - Northfield is voluntarily recalling Medline Convenience kits used for various procedures:  1) OCULOPLASTIC PICK PACK, Model Number: DYNJ43914B;   2) PLASTIC PACK, Model Number: DYNJ65109;   3) PLASTIC PROCEDURE PACK, Model Number: DYNJ34160D;   4) MINOR BREAST SJHC-LF, Model Number: DYNJ84991;   5) PLASTIC PACK, Model Number: DYNJ66056;   6) MUSCLE PLASTIC PACK, Model Number: DYNJ66212A;   7) MINOR PLASTIC PACK, Model Number: DYNJ37231B;   8) GENERAL BREAST GRH-LF, Model Number: DYNJ52658D;   9) GENERAL BREAST GRH-LF, Model Number: DYNJ52658D;   10) FACE PACK, Model Number: DYNJ37316D;   11) PLASTIC PACK-LF, Model Number: DYNJ57440D;   12) MINOR BREAST SJHC-LF, Model Number: DYNJ84991;   13) MINOR PLASTIC PACK, Model Number: DYNJ37231B;   14) SATELLITE MINOR PLASTIC PACK, Model Number: DYNJ63696;   15) FACIAL/EYE PACK, Model Number: DYNJ68328;   16) BREAST PACK, Model Number: DYNJ63753;   17) BREAST PACK, Model Number: DYNJ63753;   18) TUMMY PACK, Model Number: DYNJ64886A;   19) PLASTIC TORSO PK TEGH-LF, Model Number: DYNJ46737A;   20) PLASTIC BREAST PACK, Model Number: DYNJ40620F;   21) PLASTIC ENT PACK, Model Number: DYNJ64712B;   22) PLASTIC SURGERY SERV-DR GARAZO, Model Number: DYNJ34199A;   23) OCULOPLASTIC PICK PACK, Model Number: DYNJ43914B;   24) OCULAR PLASTICS, Model Number: DYNJ55985D;   25) TUMMY PACK, Model Number: DYNJ64886A;   26) MUSCLE PLASTIC PACK, Model Number: DYNJ66212A;   27) ZURI BREAST PACK, Model Number: DYNJ67772A;   28) PLASTIC TORSO PK TEGH-LF, Model Number: DYNJ46737A;   29) TUMMY PACK, Model Number: DYNJ64886A;   30) OCCULAR PLASTIC PACK, Model Number: DYNJ35741D;   31) FACELIFT PACK, Model Number: DYNJ38907;   32) BREAST PACK, Model Number: DYNJ67882;   33) KDOP PLASTIC PACK, Model Number: DYNJ37142D — reason: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.. Status: Ongoing — the recall is still being carried out.. Initiated 2025-03-03. Affected lots/codes: 1) DYNJ43914B, UDI-DI: 10889942437078(each), 40889942437079(case), Lot Number: 24IBH633; 2) DYNJ65109, UDI-DI: 10193489243826(each), 40193489243827(case), Lot Number: 24IBH739; 3) DYNJ34160D, UDI-DI: 10889942213542(each), 40889942213543(case), Lot Number: 24IBH802; 4) DYNJ84991, UDI-DI: 10195327444075(each), 40195327444076(case), Lot Number: 24IBL195; 5) DYNJ66056, UDI-DI: 10193489318128(each), 40193489318129(case), Lot Number: 24IBR304; 6) DYNJ66212A, UDI-DI: 10195327345075(each), 40195327345076(case), Lot Number: 24JBL025; 7) DYNJ37231B, UDI-DI: 10884389871652(each), 40884389871653(case), Lot Number: 24JBM075; 8) DYNJ52658D, UDI-DI: 10195327468828(each), 40195327468829(case), Lot Number: 24JBM318; 9) DYNJ52658D, UDI-DI: 10195327468828(each), 40195327468829(case), Lot Number: 24JBM914; 10) DYNJ37316D, UDI-DI: 10193489672763(each), 40193489672764(case), Lot Number: 24JBT528; 11) DYNJ57440D, UDI-DI: 10193489238655(each), 40193489238656(case), Lot Number: 24JBT877; 12) DYNJ84991, UDI-DI: 10195327444075(each), 40195327444076(case), Lot Number: 24JBV138; 13) DYNJ37231B, UDI-DI: 10884389871652(each), 40884389871653(case), Lot Number: 24JBV645; 14) DYNJ63696, UDI-DI: 10193489754704(each), 40193489754705(case), Lot Number: 24JBV846; 15) DYNJ68328, UDI-DI: 10193489823554(each), 40193489823555(case), Lot Number: 24JBW152; 16) DYNJ63753, UDI-DI: 10193489757330(each), 40193489757331(case), Lot Number: 24JBW480; 17) DYNJ63753, UDI-DI: 10193489757330(each), 40193489757331(case), Lot Number: 24JBX780; 18) DYNJ64886A, UDI-DI: 10193489916355(each), 40193489916356(case), Lot Number: 24JBX789; 19) DYNJ46737A, UDI-DI: 10889942116553(each), 40889942116554(case), Lot Number: 24KBA440; 20) DYNJ40620F, UDI-DI: 10195327631321(each), 40195327631322(case), Lot Number: 24KBB123; 21) DYNJ64712B, UDI-DI: 10198459166037(each), 40198459166038(case), Lot Number: 24KBB906; 22) DYNJ34199A, UDI-DI: 10884389380406(each), 40884389380407(case), Lot Number: 24KBC573; 23) DYNJ43914B, UDI-DI: 10889942437078(each), 40889942437079(case), Lot Number: 24KBC625; 24) DYNJ55985D, UDI-DI: 10193489288940(each), 40193489288941(case), Lot Number: 24KBC670; 25) DYNJ64886A, UDI-DI: 10193489916355(each), 40193489916356(case), Lot Number: 24KBC738; 26) DYNJ66212A, UDI-DI: 10195327345075(each), 40195327345076(case), Lot Number: 24KBC750; 27) DYNJ67772A, UDI-DI: 10195327209704(each), 40195327209705(case), Lot Number: 24KBC752; 28) DYNJ46737A, UDI-DI: 10889942116553(each), 40889942116554(case), Lot Number: 24KBE585; 29) DYNJ64886A, UDI-DI: 10193489916355(each), 40193489916356(case), Lot Number: 24KBF385; 30) DYNJ35741D, UDI-DI: 10889942108534(each), 40889942108535(case), Lot Number: 24KBF775; 31) DYNJ38907, UDI-DI: 10884389722176(each), 40884389722177(case), Lot Number: 24KBH241; 32) DYNJ67882, UDI-DI: 10193489449532(each), 40193489449533(case), Lot Number: 24KBH367; 33) DYNJ37142D, UDI-DI: 10195327467708(each), 40195327467709(case), Lot Number: 24KBI482. A RECORDED FDA enforcement action (occurred=true).",
      "claimType": "official_fact",
      "reviewStatus": "current",
      "commercialInfluence": false,
      "epistemicStatus": {
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        "sourceUrl": "https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=Z-1600-2025&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-1600-2025&lang=eng"
        }
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      "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-1600-2025/fda-classification",
      "@type": "schema:Claim",
      "name": "FDA classified recall Z-1600-2025 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-1600-2025&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-1600-2025&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-1600-2025/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-1600-2025",
      "numberOfItems": 9,
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          "position": 1,
          "item": {
            "Field": "Recall number",
            "Value": "Z-1600-2025",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 2,
          "item": {
            "Field": "Product type",
            "Value": "Devices",
            "Status": "recorded"
          }
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        {
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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"
          }
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          "@type": "schema:ListItem",
          "position": 5,
          "item": {
            "Field": "Recalling firm",
            "Value": "MEDLINE INDUSTRIES, LP - Northfield",
            "Status": "recorded"
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          "position": 6,
          "item": {
            "Field": "Reason",
            "Value": "There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.",
            "Status": "recorded"
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        {
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            "Field": "Initiated",
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            "Status": "recorded"
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          "item": {
            "Field": "Lot/code info",
            "Value": "1) DYNJ43914B, UDI-DI: 10889942437078(each), 40889942437079(case), Lot Number: 24IBH633; 2) DYNJ65109, UDI-DI: 10193489243826(each), 40193489243827(case), Lot Number: 24IBH739; 3) DYNJ34160D, UDI-DI: 10889942213542(each), 40889942213543(case), Lot Number: 24IBH802; 4) DYNJ84991, UDI-DI: 10195327444075(each), 40195327444076(case), Lot Number: 24IBL195; 5) DYNJ66056, UDI-DI: 10193489318128(each), 40193489318129(case), Lot Number: 24IBR304; 6) DYNJ66212A, UDI-DI: 10195327345075(each), 40195327345076(case), Lot Number: 24JBL025; 7) DYNJ37231B, UDI-DI: 10884389871652(each), 40884389871653(case), Lot Number: 24JBM075; 8) DYNJ52658D, UDI-DI: 10195327468828(each), 40195327468829(case), Lot Number: 24JBM318; 9) DYNJ52658D, UDI-DI: 10195327468828(each), 40195327468829(case), Lot Number: 24JBM914; 10) DYNJ37316D, UDI-DI: 10193489672763(each), 40193489672764(case), Lot Number: 24JBT528; 11) DYNJ57440D, UDI-DI: 10193489238655(each), 40193489238656(case), Lot Number: 24JBT877; 12) DYNJ84991, UDI-DI: 10195327444075(each), 40195327444076(case), Lot Number: 24JBV138; 13) DYNJ37231B, UDI-DI: 10884389871652(each), 40884389871653(case), Lot Number: 24JBV645; 14) DYNJ63696, UDI-DI: 10193489754704(each), 40193489754705(case), Lot Number: 24JBV846; 15) DYNJ68328, UDI-DI: 10193489823554(each), 40193489823555(case), Lot Number: 24JBW152; 16) DYNJ63753, UDI-DI: 10193489757330(each), 40193489757331(case), Lot Number: 24JBW480; 17) DYNJ63753, UDI-DI: 10193489757330(each), 40193489757331(case), Lot Number: 24JBX780; 18) DYNJ64886A, UDI-DI: 10193489916355(each), 40193489916356(case), Lot Number: 24JBX789; 19) DYNJ46737A, UDI-DI: 10889942116553(each), 40889942116554(case), Lot Number: 24KBA440; 20) DYNJ40620F, UDI-DI: 10195327631321(each), 40195327631322(case), Lot Number: 24KBB123; 21) DYNJ64712B, UDI-DI: 10198459166037(each), 40198459166038(case), Lot Number: 24KBB906; 22) DYNJ34199A, UDI-DI: 10884389380406(each), 40884389380407(case), Lot Number: 24KBC573; 23) DYNJ43914B, UDI-DI: 10889942437078(each), 40889942437079(case), Lot Number: 24KBC625; 24) DYNJ55985D, UDI-DI: 10193489288940(each), 40193489288941(case), Lot Number: 24KBC670; 25) DYNJ64886A, UDI-DI: 10193489916355(each), 40193489916356(case), Lot Number: 24KBC738; 26) DYNJ66212A, UDI-DI: 10195327345075(each), 40195327345076(case), Lot Number: 24KBC750; 27) DYNJ67772A, UDI-DI: 10195327209704(each), 40195327209705(case), Lot Number: 24KBC752; 28) DYNJ46737A, UDI-DI: 10889942116553(each), 40889942116554(case), Lot Number: 24KBE585; 29) DYNJ64886A, UDI-DI: 10193489916355(each), 40193489916356(case), Lot Number: 24KBF385; 30) DYNJ35741D, UDI-DI: 10889942108534(each), 40889942108535(case), Lot Number: 24KBF775; 31) DYNJ38907, UDI-DI: 10884389722176(each), 40884389722177(case), Lot Number: 24KBH241; 32) DYNJ67882, UDI-DI: 10193489449532(each), 40193489449533(case), Lot Number: 24KBH367; 33) DYNJ37142D, UDI-DI: 10195327467708(each), 40195327467709(case), Lot Number: 24KBI482",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 9,
          "item": {
            "Field": "Distribution pattern",
            "Value": "Worldwide distribution - US Nationwide and the countries of Canada, Mexico, Panama, Virgin Islands.",
            "Status": "recorded"
          }
        }
      ]
    }
  ]
}