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  "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-1716-2026.jsonld",
  "@type": "schema:Dataset",
  "name": "Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows:    1. CATH LAB PACK-LF, Medline SKU 00-HCT055P;   2. INTERVENTIONAL CATH LAB PK-LF, Medline SKU DYNJ0376230Q;   3. ANGIOGRAPHY CATH LAB, Medline SKU DYNJ23532C;   4. ANGIO LEFT HEART PACK, Medline SKU DYNJ40632C;   5. ANGIO DRAPE PACK, Medline SKU DYNJ47952B;   6. ANGIOGRAPHIC PACK, Medline SKU DYNJ57516;   7. CATH LAB PACK, Medline SKU DYNJ58243B;   8. CATH LAB PACK, Medline SKU DYNJ65185;   9. CSU CATH MANIFOLD KIT, Medline SKU VASC1170A;   10. MANIFOLD KIT NO TRANSDUCER, Medline SKU VASC1184A.",
  "description": "FDA recall Z-1716-2026 — Medline Industries, LP is recalling Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows:    1. CATH LAB PACK-LF, Medline SKU 00-HCT055P;   2. INTERVENTIONAL CATH LAB PK-LF, Medline SKU DYNJ0376230Q;   3. ANGIOGRAPHY CATH LAB, Medline SKU DYNJ23532C;   4. ANGIO LEFT HEART PACK, Medline SKU DYNJ40632C;   5. ANGIO DRAPE PACK, Medline SKU DYNJ47952B;   6. ANGIOGRAPHIC PACK, Medline SKU DYNJ57516;   7. CATH LAB PACK, Medline SKU DYNJ58243B;   8. CATH LAB PACK, Medline SKU DYNJ65185;   9. CSU CATH MANIFOLD KIT, Medline SKU VASC1170A;   10. MANIFOLD KIT NO TRANSDUCER, Medline SKU VASC1184A. (Devices, Class I). 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.",
  "license": "https://creativecommons.org/publicdomain/zero/1.0/",
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  "dateModified": "2026-06-24T07:02:03.626072+00:00",
  "isBasedOn": {
    "@type": "schema:Dataset",
    "name": "openFDA drug & device enforcement (recall) reports",
    "url": "https://open.fda.gov/apis/drug/enforcement/",
    "creator": {
      "@type": "schema:GovernmentOrganization",
      "name": "U.S. Food & Drug Administration"
    }
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  "sameAs": "https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=Z-1716-2026&lang=eng",
  "about": {
    "@type": "schema:MedicalDevice",
    "name": "Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows:    1. CATH LAB PACK-LF, Medline SKU 00-HCT055P;   2. INTERVENTIONAL CATH LAB PK-LF, Medline SKU DYNJ0376230Q;   3. ANGIOGRAPHY CATH LAB, Medline SKU DYNJ23532C;   4. ANGIO LEFT HEART PACK, Medline SKU DYNJ40632C;   5. ANGIO DRAPE PACK, Medline SKU DYNJ47952B;   6. ANGIOGRAPHIC PACK, Medline SKU DYNJ57516;   7. CATH LAB PACK, Medline SKU DYNJ58243B;   8. CATH LAB PACK, Medline SKU DYNJ65185;   9. CSU CATH MANIFOLD KIT, Medline SKU VASC1170A;   10. MANIFOLD KIT NO TRANSDUCER, Medline SKU VASC1184A.",
    "manufacturer": {
      "@type": "schema:Organization",
      "name": "Medline Industries, LP"
    }
  },
  "claims": [
    {
      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-1716-2026/enforcement-record",
      "@type": "schema:Claim",
      "name": "FDA recall Z-1716-2026: Medline Industries, LP is recalling Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows:    1. CATH LAB PACK-LF, Medline SKU 00-HCT055P;   2. INTERVENTIONAL CATH LAB PK-LF, Medline SKU DYNJ0376230Q;   3. ANGIOGRAPHY CATH LAB, Medline SKU DYNJ23532C;   4. ANGIO LEFT HEART PACK, Medline SKU DYNJ40632C;   5. ANGIO DRAPE PACK, Medline SKU DYNJ47952B;   6. ANGIOGRAPHIC PACK, Medline SKU DYNJ57516;   7. CATH LAB PACK, Medline SKU DYNJ58243B;   8. CATH LAB PACK, Medline SKU DYNJ65185;   9. CSU CATH MANIFOLD KIT, Medline SKU VASC1170A;   10. MANIFOLD KIT NO TRANSDUCER, Medline SKU VASC1184A.",
      "text": "The FDA logged enforcement record Z-1716-2026: Medline Industries, LP is voluntarily recalling Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows:    1. CATH LAB PACK-LF, Medline SKU 00-HCT055P;   2. INTERVENTIONAL CATH LAB PK-LF, Medline SKU DYNJ0376230Q;   3. ANGIOGRAPHY CATH LAB, Medline SKU DYNJ23532C;   4. ANGIO LEFT HEART PACK, Medline SKU DYNJ40632C;   5. ANGIO DRAPE PACK, Medline SKU DYNJ47952B;   6. ANGIOGRAPHIC PACK, Medline SKU DYNJ57516;   7. CATH LAB PACK, Medline SKU DYNJ58243B;   8. CATH LAB PACK, Medline SKU DYNJ65185;   9. CSU CATH MANIFOLD KIT, Medline SKU VASC1170A;   10. MANIFOLD KIT NO TRANSDUCER, Medline SKU VASC1184A. — reason: Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.. Status: Ongoing — the recall is still being carried out.. Initiated 2026-02-27. Affected lots/codes: Medline SKU 00-HCT055P, UDI/DI each 10193489297393, UDI/DI case 40193489297394, Lot Number 24BBI341;  Medline SKU 00-HCT055P, UDI/DI each 10193489297393, UDI/DI case 40193489297394, Lot Number 23LBP066;  Medline SKU 00-HCT055P, UDI/DI each 10193489297393, UDI/DI case 40193489297394, Lot Number 23KBS305;  Medline SKU 00-HCT055P, UDI/DI each 10193489297393, UDI/DI case 40193489297394, Lot Number 23JBA062;  Medline SKU 00-HCT055P, UDI/DI each 10193489297393, UDI/DI case 40193489297394, Lot Number 23HBR594;  Medline SKU 00-HCT055P, UDI/DI each 10193489297393, UDI/DI case 40193489297394, Lot Number 23DBR051;  Medline SKU DYNJ0376230Q, UDI/DI each 10193489759303, UDI/DI case 40193489759304, Lot Number 24ABO014;  Medline SKU DYNJ0376230Q, UDI/DI each 10193489759303, UDI/DI case 40193489759304, Lot Number 23KBW878;  Medline SKU DYNJ0376230Q, UDI/DI each 10193489759303, UDI/DI case 40193489759304, Lot Number 23HBP761;  Medline SKU DYNJ0376230Q, UDI/DI each 10193489759303, UDI/DI case 40193489759304, Lot Number 23FBW006;  Medline SKU DYNJ0376230Q, UDI/DI each 10193489759303, UDI/DI case 40193489759304, Lot Number 23DBF403;  Medline SKU DYNJ23532C, UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 25KMD905;  Medline SKU DYNJ23532C, UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 25IMD215;  Medline SKU DYNJ23532C, UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 25GMI326;  Medline SKU DYNJ23532C, UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 25FMI653;  Medline SKU DYNJ23532C, UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 25EMH566;  Medline SKU DYNJ23532C, UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 25DMI277;  Medline SKU DYNJ23532C, UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 25AMI608;  Medline SKU DYNJ23532C, UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 24LMH838;  Medline SKU DYNJ23532C, UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 24LMB458;  Medline SKU DYNJ23532C, UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 24JME629;  Medline SKU DYNJ23532C, UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 24GME647;  Medline SKU DYNJ23532C, UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 24GMB984;  Medline SKU DYNJ23532C, UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 24GMB351;  Medline SKU DYNJ23532C, UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 24EMF938;  Medline SKU DYNJ23532C, UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 24DMH385;  Medline SKU DYNJ23532C, UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 24CMH336;  Medline SKU DYNJ23532C, UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 24CMF956;  Medline SKU DYNJ23532C, UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 24BMA898;  Medline SKU DYNJ23532C, UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 24AMA108;  Medline SKU DYNJ23532C, UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 23HMH132;  Medline SKU DYNJ23532C, UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 23GMH036;  Medline SKU DYNJ23532C, UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 23GME698;  Medline SKU DYNJ23532C, UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 23FMF802;  Medline SKU DYNJ23532C, UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 23EMJ218;  Medline SKU DYNJ40632C, UDI/DI each 10193489461176, UDI/DI case 40193489461177, Lot Number 24JMD976;  Medline SKU DYNJ40632C, UDI/DI each 10193489461176, UDI/DI case 40193489461177, Lot Number 24HMA010;  Medline SKU DYNJ40632C, UDI/DI each 10193489461176, UDI/DI case 40193489461177, Lot Number 24GMG026;  Medline SKU DYNJ40632C, UDI/DI each 10193489461176, UDI/DI case 40193489461177, Lot Number 24GMB098;  Medline SKU DYNJ40632C, UDI/DI each 10193489461176, UDI/DI case 40193489461177, Lot Number 24FMF601;  Medline SKU DYNJ40632C, UDI/DI each 10193489461176, UDI/DI case 40193489461177, Lot Number 24EMB438;  Medline SKU DYNJ40632C, UDI/DI each 10193489461176, UDI/DI case 40193489461177, Lot Number 24BMA764;  Medline SKU DYNJ40632C, UDI/DI each 10193489461176, UDI/DI case 40193489461177, Lot Number 23LME233;  Medline SKU DYNJ40632C, UDI/DI each 10193489461176, UDI/DI case 40193489461177, Lot Number 23JMH698;  Medline SKU DYNJ40632C, UDI/DI each 10193489461176, UDI/DI case 40193489461177, Lot Number 23IMD171;  Medline SKU DYNJ40632C, UDI/DI each 10193489461176, UDI/DI case 40193489461177, Lot Number 23GMD850;  Medline SKU DYNJ40632C, UDI/DI each 10193489461176, UDI/DI case 40193489461177, Lot Number 23FMF778;  Medline SKU DYNJ40632C, UDI/DI each 10193489461176, UDI/DI case 40193489461177, Lot Number 23EMG560;  Medline SKU DYNJ47952B, UDI/DI each 10193489609851, UDI/DI case 40193489609852, Lot Number 25LMG779;  Medline SKU DYNJ47952B, UDI/DI each 10193489609851, UDI/DI case 40193489609852, Lot Number 25IMJ214;  Medline SKU DYNJ47952B, UDI/DI each 10193489609851, UDI/DI case 40193489609852, Lot Number 25HMF990;  Medline SKU DYNJ47952B, UDI/DI each 10193489609851, UDI/DI case 40193489609852, Lot Number 25EMI063;  Medline SKU DYNJ47952B, UDI/DI each 10193489609851, UDI/DI case 40193489609852, Lot Number 25DMB127;  Medline SKU DYNJ47952B, UDI/DI each 10193489609851, UDI/DI case 40193489609852, Lot Number 25BMF602;  Medline SKU DYNJ47952B, UDI/DI each 10193489609851, UDI/DI case 40193489609852, Lot Number 24LMF104;  Medline SKU DYNJ47952B, UDI/DI each 10193489609851, UDI/DI case 40193489609852, Lot Number 24KMD144;  Medline SKU DYNJ47952B, UDI/DI each 10193489609851, UDI/DI case 40193489609852, Lot Number 24JMA170;  Medline SKU DYNJ47952B, UDI/DI each 10193489609851, UDI/DI case 40193489609852, Lot Number 24HMH276;  Medline SKU DYNJ47952B, UDI/DI each 10193489609851, UDI/DI case 40193489609852, Lot Number 24HMA390;  Medline SKU DYNJ47952B, UDI/DI each 10193489609851, UDI/DI case 40193489609852, Lot Number 24FMD853;  Medline SKU DYNJ47952B, UDI/DI each 10193489609851, UDI/DI case 40193489609852, Lot Number 24DMJ147;  Medline SKU DYNJ47952B, UDI/DI each 10193489609851, UDI/DI case 40193489609852, Lot Number 24CMH759;  Medline SKU DYNJ47952B, UDI/DI each 10193489609851, UDI/DI case 40193489609852, Lot Number 24BMA225;  Medline SKU DYNJ47952B, UDI/DI each 10193489609851, UDI/DI case 40193489609852, Lot Number 23LMB166;  Medline SKU DYNJ47952B, UDI/DI each 10193489609851, UDI/DI case 40193489609852, Lot Number 23KMH325;  Medline SKU DYNJ47952B, UDI/DI each 10193489609851, UDI/DI case 40193489609852, Lot Number 23IME127;  Medline SKU DYNJ47952B, UDI/DI each 10193489609851, UDI/DI case 40193489609852, Lot Number 23HME466;  Medline SKU DYNJ47952B, UDI/DI each 10193489609851, UDI/DI case 40193489609852, Lot Number 23FMJ772;  Medline SKU DYNJ47952B, UDI/DI each 10193489609851, UDI/DI case 40193489609852, Lot Number 23FMB456;  Medline SKU DYNJ47952B, UDI/DI each 10193489609851, UDI/DI case 40193489609852, Lot Number 23EMC182;  Medline SKU DYNJ47952B, UDI/DI each 10193489609851, UDI/DI case 40193489609852, Lot Number 23DMH934;  Medline SKU DYNJ57516, UDI/DI each 10889942748426, UDI/DI case 40889942748427, Lot Number 25JMI272;  Medline SKU DYNJ57516, UDI/DI each 10889942748426, UDI/DI case 40889942748427, Lot Number 25HMG164;  Medline SKU DYNJ57516, UDI/DI each 10889942748426, UDI/DI case 40889942748427, Lot Number 25HMF202;  Medline SKU DYNJ58243B, UDI/DI each 10193489791860, UDI/DI case 40193489791861, Lot Number 25LBB437;  Medline SKU DYNJ58243B, UDI/DI each 10193489791860, UDI/DI case 40193489791861, Lot Number 25HBV263;  Medline SKU DYNJ58243B, UDI/DI each 10193489791860, UDI/DI case 40193489791861, Lot Number 25GBR191;  Medline SKU DYNJ58243B, UDI/DI each 10193489791860, UDI/DI case 40193489791861, Lot Number 25GBR194;  Medline SKU DYNJ58243B, UDI/DI each 10193489791860, UDI/DI case 40193489791861, Lot Number 25GBR437;  Medline SKU DYNJ58243B, UDI/DI each 10193489791860, UDI/DI case 40193489791861, Lot Number 25EBO829;  Medline SKU DYNJ58243B, UDI/DI each 10193489791860, UDI/DI case 40193489791861, Lot Number 25BBR177;  Medline SKU DYNJ58243B, UDI/DI each 10193489791860, UDI/DI case 40193489791861, Lot Number 24JBX749;  Medline SKU DYNJ58243B, UDI/DI each 10193489791860, UDI/DI case 40193489791861, Lot Number 24JBG123;  Medline SKU DYNJ58243B, UDI/DI each 10193489791860, UDI/DI case 40193489791861, Lot Number 24IBJ506;  Medline SKU DYNJ58243B, UDI/DI each 10193489791860, UDI/DI case 40193489791861, Lot Number 24FBT677;  Medline SKU DYNJ58243B, UDI/DI each 10193489791860, UDI/DI case 40193489791861, Lot Number 24FBH497;  Medline SKU DYNJ58243B, UDI/DI each 10193489791860, UDI/DI case 40193489791861, Lot Number 24DBL409;  Medline SKU DYNJ58243B, UDI/DI each 10193489791860, UDI/DI case 40193489791861, Lot Number 24BBT394;  Medline SKU DYNJ58243B, UDI/DI each 10193489791860, UDI/DI case 40193489791861, Lot Number 24ABR246;  Medline SKU DYNJ58243B, UDI/DI each 10193489791860, UDI/DI case 40193489791861, Lot Number 23LBK160;  Medline SKU DYNJ58243B, UDI/DI each 10193489791860, UDI/DI case 40193489791861, Lot Number 23KBJ685;  Medline SKU DYNJ58243B, UDI/DI each 10193489791860, UDI/DI case 40193489791861, Lot Number 23IBU014;  Medline SKU DYNJ58243B, UDI/DI each 10193489791860, UDI/DI case 40193489791861, Lot Number 23IBG647;  Medline SKU DYNJ58243B, UDI/DI each 10193489791860, UDI/DI case 40193489791861, Lot Number 23HBB827;  Medline SKU DYNJ58243B, UDI/DI each 10193489791860, UDI/DI case 40193489791861, Lot Number 23FBU409;  Medline SKU DYNJ65185, UDI/DI each 10193489253146, UDI/DI case 40193489253147, Lot Number 24ABQ959;  Medline SKU DYNJ65185, UDI/DI each 10193489253146, UDI/DI case 40193489253147, Lot Number 23KBF277;  Medline SKU DYNJ65185, UDI/DI each 10193489253146, UDI/DI case 40193489253147, Lot Number 23IBR043;  Medline SKU DYNJ65185, UDI/DI each 10193489253146, UDI/DI case 40193489253147, Lot Number 23HBI873;  Medline SKU DYNJ65185, UDI/DI each 10193489253146, UDI/DI case 40193489253147, Lot Number 23GBA252;  Medline SKU DYNJ65185, UDI/DI each 10193489253146, UDI/DI case 40193489253147, Lot Number 23EBM886;  Medline SKU VASC1170A, UDI/DI each 10193489774863, UDI/DI case 40193489774864, Lot Number 25HMD546;  Medline SKU VASC1184A, UDI/DI each 10193489799828, UDI/DI case 40193489799829, Lot Number 25HBL365;  Medline SKU VASC1184A, UDI/DI each 10193489799828, UDI/DI case 40193489799829, Lot Number 25GBL071;  Medline SKU VASC1184A, UDI/DI each 10193489799828, UDI/DI case 40193489799829, Lot Number 24GBY914.. A RECORDED FDA enforcement action (occurred=true).",
      "claimType": "official_fact",
      "reviewStatus": "current",
      "commercialInfluence": false,
      "epistemicStatus": {
        "occurred": true,
        "supported": true,
        "adjudged": true,
        "operative": true
      },
      "grounding": {
        "groundingType": "SourceCitation",
        "source": "openFDA drug & device enforcement (recall) reports — U.S. FDA",
        "sourceUrl": "https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=Z-1716-2026&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-1716-2026&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-1716-2026/fda-classification",
      "@type": "schema:Claim",
      "name": "FDA classified recall Z-1716-2026 as Class I",
      "text": "The FDA assigned this recall Class I: Class I — the FDA judged there is a reasonable probability that use of the product would cause serious harm or death.. 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-1716-2026&lang=eng",
        "value": "Class I",
        "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-1716-2026&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-1716-2026/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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      "numberOfItems": 9,
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          "position": 1,
          "item": {
            "Field": "Recall number",
            "Value": "Z-1716-2026",
            "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 I",
            "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",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 6,
          "item": {
            "Field": "Reason",
            "Value": "Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 7,
          "item": {
            "Field": "Initiated",
            "Value": "2026-02-27",
            "Status": "recorded"
          }
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            "Status": "recorded"
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          "item": {
            "Field": "Distribution pattern",
            "Value": "Worldwide distribution: US (nationwide) including Puerto Rico (PR) and OUS (foreign) to countries of: Canada (CA), Netherlands (NL), Australia (AU), Korea, Republic of (KR), Sri Lanka (LK), Pakistan (PK), Japan (JP), United Arab Emirates (AE), Singapore (SG) and Slovakia (SK).",
            "Status": "recorded"
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}