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  "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-1200-2026.jsonld",
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  "name": "Medline medical procedure convenience kits labeled as:    1)\tWATKINS SPINE PACK-LF, Kit SKU DYNJ0275635M;   2)\tSM-SPINE PACK-LF, Kit SKU DYNJ0395037X;   3)\tTOTAL HIP PACK, Kit SKU DYNJ04809N;   4)\tMAIN/LAMINECTOMY PACK-LF, Kit SKU DYNJ0565499AN;   5)\tSCC/SPOC HAND & FOOT PACK, Kit SKU DYNJ27164Q;   6)\tORTHO SPINE, Kit SKU DYNJ40221G;   7)\tURO GYN PACK, Kit SKU DYNJ45311J;   8)\tLAMINECTOMY PACK, Kit SKU DYNJ46330C;   9)\tDJ ORTHO SPINE, Kit SKU DYNJ48980M;   10)\tCERVICAL PACK, Kit SKU DYNJ52995F;   11)\tNORTH BACK FUSION PACK-LF, Kit SKU DYNJ56483L;   12)\tKNEE ARTHROSCOPY CHRISTUS, Kit SKU DYNJ61200B;   13)\tKNEE ARTHROSCOPY PACK-LF, Kit SKU DYNJ66150;   14)\tHIP PACK, Kit SKU DYNJ66630;   15)\tOHNS FREE FLAP A PACK, Kit SKU DYNJ69065F;   16)\tLUMBAR PACK, Kit SKU DYNJ69113C;   17)\tLAMINECTOMY PACK, Kit SKU DYNJ69401D;   18)\tLAMINECTOMY PACK, Kit SKU DYNJ81013D;   19)\tHIP/SHOULDER ARTHROSCOPY PACK, Kit SKU DYNJ84275A;   20)\tFLASC ACL PACK, Kit SKU DYNJ88971;   21)\tSPINE PACK MERCY GALENA, Kit SKU DYNJ89943;   22)\tSPINAL FUSION MT CARMEL, Kit SKU DYNJ900173J;   23)\tHAND, Kit SKU DYNJ904945G;   24)\tLAMINECTOMY, Kit SKU DYNJ909505D;   25)\tSHOULDER SPLIT, Kit SKU DYNJ910543F;   26)\tSHOULDER SPLIT, Kit SKU DYNJ910543G;   27)\tCRANIOTOMY PACK, Kit SKU DYNJT4724;   28)\tSPINE PACK, Kit SKU DYNJT5184.",
  "description": "FDA recall Z-1200-2026 — Medline Industries, LP is recalling Medline medical procedure convenience kits labeled as:    1)\tWATKINS SPINE PACK-LF, Kit SKU DYNJ0275635M;   2)\tSM-SPINE PACK-LF, Kit SKU DYNJ0395037X;   3)\tTOTAL HIP PACK, Kit SKU DYNJ04809N;   4)\tMAIN/LAMINECTOMY PACK-LF, Kit SKU DYNJ0565499AN;   5)\tSCC/SPOC HAND & FOOT PACK, Kit SKU DYNJ27164Q;   6)\tORTHO SPINE, Kit SKU DYNJ40221G;   7)\tURO GYN PACK, Kit SKU DYNJ45311J;   8)\tLAMINECTOMY PACK, Kit SKU DYNJ46330C;   9)\tDJ ORTHO SPINE, Kit SKU DYNJ48980M;   10)\tCERVICAL PACK, Kit SKU DYNJ52995F;   11)\tNORTH BACK FUSION PACK-LF, Kit SKU DYNJ56483L;   12)\tKNEE ARTHROSCOPY CHRISTUS, Kit SKU DYNJ61200B;   13)\tKNEE ARTHROSCOPY PACK-LF, Kit SKU DYNJ66150;   14)\tHIP PACK, Kit SKU DYNJ66630;   15)\tOHNS FREE FLAP A PACK, Kit SKU DYNJ69065F;   16)\tLUMBAR PACK, Kit SKU DYNJ69113C;   17)\tLAMINECTOMY PACK, Kit SKU DYNJ69401D;   18)\tLAMINECTOMY PACK, Kit SKU DYNJ81013D;   19)\tHIP/SHOULDER ARTHROSCOPY PACK, Kit SKU DYNJ84275A;   20)\tFLASC ACL PACK, Kit SKU DYNJ88971;   21)\tSPINE PACK MERCY GALENA, Kit SKU DYNJ89943;   22)\tSPINAL FUSION MT CARMEL, Kit SKU DYNJ900173J;   23)\tHAND, Kit SKU DYNJ904945G;   24)\tLAMINECTOMY, Kit SKU DYNJ909505D;   25)\tSHOULDER SPLIT, Kit SKU DYNJ910543F;   26)\tSHOULDER SPLIT, Kit SKU DYNJ910543G;   27)\tCRANIOTOMY PACK, Kit SKU DYNJT4724;   28)\tSPINE PACK, Kit SKU DYNJT5184. (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 medical procedure convenience kits labeled as:    1)\tWATKINS SPINE PACK-LF, Kit SKU DYNJ0275635M;   2)\tSM-SPINE PACK-LF, Kit SKU DYNJ0395037X;   3)\tTOTAL HIP PACK, Kit SKU DYNJ04809N;   4)\tMAIN/LAMINECTOMY PACK-LF, Kit SKU DYNJ0565499AN;   5)\tSCC/SPOC HAND & FOOT PACK, Kit SKU DYNJ27164Q;   6)\tORTHO SPINE, Kit SKU DYNJ40221G;   7)\tURO GYN PACK, Kit SKU DYNJ45311J;   8)\tLAMINECTOMY PACK, Kit SKU DYNJ46330C;   9)\tDJ ORTHO SPINE, Kit SKU DYNJ48980M;   10)\tCERVICAL PACK, Kit SKU DYNJ52995F;   11)\tNORTH BACK FUSION PACK-LF, Kit SKU DYNJ56483L;   12)\tKNEE ARTHROSCOPY CHRISTUS, Kit SKU DYNJ61200B;   13)\tKNEE ARTHROSCOPY PACK-LF, Kit SKU DYNJ66150;   14)\tHIP PACK, Kit SKU DYNJ66630;   15)\tOHNS FREE FLAP A PACK, Kit SKU DYNJ69065F;   16)\tLUMBAR PACK, Kit SKU DYNJ69113C;   17)\tLAMINECTOMY PACK, Kit SKU DYNJ69401D;   18)\tLAMINECTOMY PACK, Kit SKU DYNJ81013D;   19)\tHIP/SHOULDER ARTHROSCOPY PACK, Kit SKU DYNJ84275A;   20)\tFLASC ACL PACK, Kit SKU DYNJ88971;   21)\tSPINE PACK MERCY GALENA, Kit SKU DYNJ89943;   22)\tSPINAL FUSION MT CARMEL, Kit SKU DYNJ900173J;   23)\tHAND, Kit SKU DYNJ904945G;   24)\tLAMINECTOMY, Kit SKU DYNJ909505D;   25)\tSHOULDER SPLIT, Kit SKU DYNJ910543F;   26)\tSHOULDER SPLIT, Kit SKU DYNJ910543G;   27)\tCRANIOTOMY PACK, Kit SKU DYNJT4724;   28)\tSPINE PACK, Kit SKU DYNJT5184.",
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      "name": "Medline Industries, LP"
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    {
      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-1200-2026/enforcement-record",
      "@type": "schema:Claim",
      "name": "FDA recall Z-1200-2026: Medline Industries, LP is recalling Medline medical procedure convenience kits labeled as:    1)\tWATKINS SPINE PACK-LF, Kit SKU DYNJ0275635M;   2)\tSM-SPINE PACK-LF, Kit SKU DYNJ0395037X;   3)\tTOTAL HIP PACK, Kit SKU DYNJ04809N;   4)\tMAIN/LAMINECTOMY PACK-LF, Kit SKU DYNJ0565499AN;   5)\tSCC/SPOC HAND & FOOT PACK, Kit SKU DYNJ27164Q;   6)\tORTHO SPINE, Kit SKU DYNJ40221G;   7)\tURO GYN PACK, Kit SKU DYNJ45311J;   8)\tLAMINECTOMY PACK, Kit SKU DYNJ46330C;   9)\tDJ ORTHO SPINE, Kit SKU DYNJ48980M;   10)\tCERVICAL PACK, Kit SKU DYNJ52995F;   11)\tNORTH BACK FUSION PACK-LF, Kit SKU DYNJ56483L;   12)\tKNEE ARTHROSCOPY CHRISTUS, Kit SKU DYNJ61200B;   13)\tKNEE ARTHROSCOPY PACK-LF, Kit SKU DYNJ66150;   14)\tHIP PACK, Kit SKU DYNJ66630;   15)\tOHNS FREE FLAP A PACK, Kit SKU DYNJ69065F;   16)\tLUMBAR PACK, Kit SKU DYNJ69113C;   17)\tLAMINECTOMY PACK, Kit SKU DYNJ69401D;   18)\tLAMINECTOMY PACK, Kit SKU DYNJ81013D;   19)\tHIP/SHOULDER ARTHROSCOPY PACK, Kit SKU DYNJ84275A;   20)\tFLASC ACL PACK, Kit SKU DYNJ88971;   21)\tSPINE PACK MERCY GALENA, Kit SKU DYNJ89943;   22)\tSPINAL FUSION MT CARMEL, Kit SKU DYNJ900173J;   23)\tHAND, Kit SKU DYNJ904945G;   24)\tLAMINECTOMY, Kit SKU DYNJ909505D;   25)\tSHOULDER SPLIT, Kit SKU DYNJ910543F;   26)\tSHOULDER SPLIT, Kit SKU DYNJ910543G;   27)\tCRANIOTOMY PACK, Kit SKU DYNJT4724;   28)\tSPINE PACK, Kit SKU DYNJT5184.",
      "text": "The FDA logged enforcement record Z-1200-2026: Medline Industries, LP is voluntarily recalling Medline medical procedure convenience kits labeled as:    1)\tWATKINS SPINE PACK-LF, Kit SKU DYNJ0275635M;   2)\tSM-SPINE PACK-LF, Kit SKU DYNJ0395037X;   3)\tTOTAL HIP PACK, Kit SKU DYNJ04809N;   4)\tMAIN/LAMINECTOMY PACK-LF, Kit SKU DYNJ0565499AN;   5)\tSCC/SPOC HAND & FOOT PACK, Kit SKU DYNJ27164Q;   6)\tORTHO SPINE, Kit SKU DYNJ40221G;   7)\tURO GYN PACK, Kit SKU DYNJ45311J;   8)\tLAMINECTOMY PACK, Kit SKU DYNJ46330C;   9)\tDJ ORTHO SPINE, Kit SKU DYNJ48980M;   10)\tCERVICAL PACK, Kit SKU DYNJ52995F;   11)\tNORTH BACK FUSION PACK-LF, Kit SKU DYNJ56483L;   12)\tKNEE ARTHROSCOPY CHRISTUS, Kit SKU DYNJ61200B;   13)\tKNEE ARTHROSCOPY PACK-LF, Kit SKU DYNJ66150;   14)\tHIP PACK, Kit SKU DYNJ66630;   15)\tOHNS FREE FLAP A PACK, Kit SKU DYNJ69065F;   16)\tLUMBAR PACK, Kit SKU DYNJ69113C;   17)\tLAMINECTOMY PACK, Kit SKU DYNJ69401D;   18)\tLAMINECTOMY PACK, Kit SKU DYNJ81013D;   19)\tHIP/SHOULDER ARTHROSCOPY PACK, Kit SKU DYNJ84275A;   20)\tFLASC ACL PACK, Kit SKU DYNJ88971;   21)\tSPINE PACK MERCY GALENA, Kit SKU DYNJ89943;   22)\tSPINAL FUSION MT CARMEL, Kit SKU DYNJ900173J;   23)\tHAND, Kit SKU DYNJ904945G;   24)\tLAMINECTOMY, Kit SKU DYNJ909505D;   25)\tSHOULDER SPLIT, Kit SKU DYNJ910543F;   26)\tSHOULDER SPLIT, Kit SKU DYNJ910543G;   27)\tCRANIOTOMY PACK, Kit SKU DYNJT4724;   28)\tSPINE PACK, Kit SKU DYNJT5184. — reason: Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.. Status: Ongoing — the recall is still being carried out.. Initiated 2025-12-12. Affected lots/codes: Medline Kit SKU DYNJ0275635M:  UDI/DI 10198459464799 (EA) 40198459464790 (CS), Lot Number 25KMH120;  Medline Kit SKU DYNJ0395037X:  UDI/DI 10198459600555 (EA) 40198459600556 (CS), Lot Number 25LMB119;  Medline Kit SKU DYNJ04809N:  UDI/DI 10198459440908 (EA) 40198459440909 (CS), Lot Number 25KMF969;  Medline Kit SKU DYNJ0565499AN:  UDI/DI 10195327318352 (EA) 40195327318353 (CS), Lot Number 25JMF339;  Medline Kit SKU DYNJ0565499AN:  UDI/DI 10195327318352 (EA) 40195327318353 (CS), Lot Number 25LMB019;  Medline Kit SKU DYNJ27164Q:  UDI/DI 10198459138102 (EA) 40198459138103 (CS), Lot Number 25KMJ742;  Medline Kit SKU DYNJ40221G:  UDI/DI 10198459448515 (EA) 40198459448516 (CS), Lot Number 25KME669;  Medline Kit SKU DYNJ45311J:  UDI/DI 10198459255670 (EA) 40198459255671 (CS), Lot Number 25KMI080;  Medline Kit SKU DYNJ46330C:  UDI/DI 10889942490066 (EA) 40889942490067 (CS), Lot Number 25KMD795;  Medline Kit SKU DYNJ48980M:  UDI/DI 10195327533694 (EA) 40195327533695 (CS), Lot Number 25KMC459;  Medline Kit SKU DYNJ52995F:  UDI/DI 10195327639778 (EA) 40195327639779 (CS), Lot Number 25KME064;  Medline Kit SKU DYNJ56483L:  UDI/DI 10195327518141 (EA) 40195327518142 (CS), Lot Number 25LMB049;  Medline Kit SKU DYNJ61200B:  UDI/DI 10195327604264 (EA) 40195327604265 (CS), Lot Number 25KBE867;  Medline Kit SKU DYNJ66150:  UDI/DI 10193489317558 (EA) 40193489317559 (CS), Lot Number 25KMC057;  Medline Kit SKU DYNJ66630:  UDI/DI 10193489368284 (EA) 40193489368285 (CS), Lot Number 25KMG435;  Medline Kit SKU DYNJ69065F:  UDI/DI 10198459226618 (EA) 40198459226619 (CS), Lot Number 25KMI293;  Medline Kit SKU DYNJ69113C:  UDI/DI 10198459170225 (EA) 40198459170226 (CS), Lot Number 25JMJ726;  Medline Kit SKU DYNJ69401D:  UDI/DI 10198459183676 (EA) 40198459183677 (CS), Lot Number 25KMJ106;  Medline Kit SKU DYNJ81013D:  UDI/DI 10198459547706 (EA) 40198459547707 (CS), Lot Number 25LDA122;  Medline Kit SKU DYNJ84275A:  UDI/DI 10198459240171 (EA) 40198459240172 (CS), Lot Number 25LMB546;  Medline Kit SKU DYNJ88971:  UDI/DI 10198459222269 (EA) 40198459222260 (CS), Lot Number 25KMH340;  Medline Kit SKU DYNJ89943:  UDI/DI 10198459299483 (EA) 40198459299484 (CS), Lot Number 25KMB583;  Medline Kit SKU DYNJ900173J:  UDI/DI 10198459292170 (EA) 40198459292171 (CS), Lot Number 25JDB487;  Medline Kit SKU DYNJ904945G:  UDI/DI 10198459518317 (EA) 40198459518318 (CS), Lot Number 25LBC198;  Medline Kit SKU DYNJ909505D:  UDI/DI 10198459594229 (EA) 40198459594220 (CS), Lot Number 25LMB637;  Medline Kit SKU DYNJ910543F:  UDI/DI 10198459554971 (EA) 40198459554972 (CS), Lot Number 25KMH376;  Medline Kit SKU DYNJ910543G:  UDI/DI 10198459588204 (EA) 40198459588205 (CS), Lot Number 25LMA619;  Medline Kit SKU DYNJT4724:  UDI/DI 10198459457913 (EA) 40198459457914 (CS), Lot Number 25KMI923;  Medline Kit SKU DYNJT5184:  UDI/DI 10198459467592 (EA) 40198459467593 (CS), Lot Number 25KMG240.. A RECORDED FDA enforcement action (occurred=true).",
      "claimType": "official_fact",
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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-1200-2026&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-1200-2026&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-1200-2026/fda-classification",
      "@type": "schema:Claim",
      "name": "FDA classified recall Z-1200-2026 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": {
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        "supported": true,
        "adjudged": true,
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        "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-1200-2026&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-1200-2026&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-1200-2026/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-1200-2026",
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          "position": 1,
          "item": {
            "Field": "Recall number",
            "Value": "Z-1200-2026",
            "Status": "recorded"
          }
        },
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          "@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",
            "Status": "recorded"
          }
        },
        {
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          "position": 6,
          "item": {
            "Field": "Reason",
            "Value": "Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 7,
          "item": {
            "Field": "Initiated",
            "Value": "2025-12-12",
            "Status": "recorded"
          }
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          "item": {
            "Field": "Lot/code info",
            "Value": "Medline Kit SKU DYNJ0275635M:  UDI/DI 10198459464799 (EA) 40198459464790 (CS), Lot Number 25KMH120;  Medline Kit SKU DYNJ0395037X:  UDI/DI 10198459600555 (EA) 40198459600556 (CS), Lot Number 25LMB119;  Medline Kit SKU DYNJ04809N:  UDI/DI 10198459440908 (EA) 40198459440909 (CS), Lot Number 25KMF969;  Medline Kit SKU DYNJ0565499AN:  UDI/DI 10195327318352 (EA) 40195327318353 (CS), Lot Number 25JMF339;  Medline Kit SKU DYNJ0565499AN:  UDI/DI 10195327318352 (EA) 40195327318353 (CS), Lot Number 25LMB019;  Medline Kit SKU DYNJ27164Q:  UDI/DI 10198459138102 (EA) 40198459138103 (CS), Lot Number 25KMJ742;  Medline Kit SKU DYNJ40221G:  UDI/DI 10198459448515 (EA) 40198459448516 (CS), Lot Number 25KME669;  Medline Kit SKU DYNJ45311J:  UDI/DI 10198459255670 (EA) 40198459255671 (CS), Lot Number 25KMI080;  Medline Kit SKU DYNJ46330C:  UDI/DI 10889942490066 (EA) 40889942490067 (CS), Lot Number 25KMD795;  Medline Kit SKU DYNJ48980M:  UDI/DI 10195327533694 (EA) 40195327533695 (CS), Lot Number 25KMC459;  Medline Kit SKU DYNJ52995F:  UDI/DI 10195327639778 (EA) 40195327639779 (CS), Lot Number 25KME064;  Medline Kit SKU DYNJ56483L:  UDI/DI 10195327518141 (EA) 40195327518142 (CS), Lot Number 25LMB049;  Medline Kit SKU DYNJ61200B:  UDI/DI 10195327604264 (EA) 40195327604265 (CS), Lot Number 25KBE867;  Medline Kit SKU DYNJ66150:  UDI/DI 10193489317558 (EA) 40193489317559 (CS), Lot Number 25KMC057;  Medline Kit SKU DYNJ66630:  UDI/DI 10193489368284 (EA) 40193489368285 (CS), Lot Number 25KMG435;  Medline Kit SKU DYNJ69065F:  UDI/DI 10198459226618 (EA) 40198459226619 (CS), Lot Number 25KMI293;  Medline Kit SKU DYNJ69113C:  UDI/DI 10198459170225 (EA) 40198459170226 (CS), Lot Number 25JMJ726;  Medline Kit SKU DYNJ69401D:  UDI/DI 10198459183676 (EA) 40198459183677 (CS), Lot Number 25KMJ106;  Medline Kit SKU DYNJ81013D:  UDI/DI 10198459547706 (EA) 40198459547707 (CS), Lot Number 25LDA122;  Medline Kit SKU DYNJ84275A:  UDI/DI 10198459240171 (EA) 40198459240172 (CS), Lot Number 25LMB546;  Medline Kit SKU DYNJ88971:  UDI/DI 10198459222269 (EA) 40198459222260 (CS), Lot Number 25KMH340;  Medline Kit SKU DYNJ89943:  UDI/DI 10198459299483 (EA) 40198459299484 (CS), Lot Number 25KMB583;  Medline Kit SKU DYNJ900173J:  UDI/DI 10198459292170 (EA) 40198459292171 (CS), Lot Number 25JDB487;  Medline Kit SKU DYNJ904945G:  UDI/DI 10198459518317 (EA) 40198459518318 (CS), Lot Number 25LBC198;  Medline Kit SKU DYNJ909505D:  UDI/DI 10198459594229 (EA) 40198459594220 (CS), Lot Number 25LMB637;  Medline Kit SKU DYNJ910543F:  UDI/DI 10198459554971 (EA) 40198459554972 (CS), Lot Number 25KMH376;  Medline Kit SKU DYNJ910543G:  UDI/DI 10198459588204 (EA) 40198459588205 (CS), Lot Number 25LMA619;  Medline Kit SKU DYNJT4724:  UDI/DI 10198459457913 (EA) 40198459457914 (CS), Lot Number 25KMI923;  Medline Kit SKU DYNJT5184:  UDI/DI 10198459467592 (EA) 40198459467593 (CS), Lot Number 25KMG240.",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 9,
          "item": {
            "Field": "Distribution pattern",
            "Value": "US Nationwide distribution.",
            "Status": "recorded"
          }
        }
      ]
    }
  ]
}