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  "name": "Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082070",
  "description": "FDA recall Z-1888-2023 — TELEFLEX LLC is recalling Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082070 (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.",
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      "name": "FDA recall Z-1888-2023: TELEFLEX LLC is recalling Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082070",
      "text": "The FDA logged enforcement record Z-1888-2023: TELEFLEX LLC is voluntarily recalling Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082070 — reason: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.. Status: Ongoing — the recall is still being carried out.. Initiated 2023-05-25. Affected lots/codes: UDI/DI 14026704341426, Batch Numbers:  18FG12, 18GG07, 18GG08, 18GG10, 18GG12, 18GG19, 18GG22, 18GT07, 18GT08, 18GT12, 18HG28, 18HG34, 18HT07, 18HT08, 18HT31, 18IG01, 18IG04, 18IG07, 18IG09, 18IG10, 18IG11, 18IG15, 18IG16, 18IG23, 18IT18, 18IT23, 18JG04, 18KG07, 18KG10, 18KG25, 18KT03, 18LG11, 18LG35, 18LG40, 19AG02, 19AG03, 19AT16, 19BG02, 19BG14, 19BG16, 19BG19, 19BG21, 19BG22, 19BG23, 19BG26, 19BG33, 19BG34, 19BG37, 19BG42, 19BT12, 19BT16, 19BT18, 19CG01, 19CG03, 19CG06, 19CT03, 19CT22, 19CT82, 19DT17, 19DT20, 19DT29, 19DT36, 19DT46, 19DT47, 19ET02, 19ET11, 19ET12, 19ET18, 19ET29, 19ET31, 19ET36, 19ET40, 19ET47, 19ET49, 19ET78, 19ET82, 19FT04, 19FT38, 19FT50, 19GT38, 19GT47, 19GT59, 19GT65, 19HT08, 19HT14, 19HT22, 19HT23, 19HT25, 19HT47, 19HT50, 19HT52, 19HT66, 19HT82, 19IT02, 19IT04, 19IT15, 19IT31, 19KT30, 19KT31, 19LT37, 20AT05, 20AT11, 20AT25, 20AT26, 20AT27, 20AT32, 20AT38, 20AT49, 20BG14, 20BT02, 20BT13, 20BT22, 20BT27, 20BT31, 20BT37, 20BT38, 20BT46, 20BT51, 20BT52, 20BT53, 20CT07, 20DT23, 20DT40, 20ET12, 20ET15, 20ET17, 20FT27, 20FT34, 20FT39, 20FT43, 20FT45, 20FT53, 20FT66, 20FT71, 20GT09, 20GT12, 20GT18, 20GT31, 20GT32, KME20H0916, KME20H1131, KME20H1244, KME20H1245, KME20H1634, KME20J2874, KME20J2896, KME20J2901, KME20J2942, KME20J3266, KME20K0061, KME20K0462, KME20K0585, KME20K1007, KME20K3013, KME20K3014, KME20K3145, KME20K3365, KME20L1691, KME20L1752, KME20L1858, KME20L2111, KME20L2210, KME20L2373, KME20L2463, KME20L2478, KME20L2499, KME20L2699, KME20M0490, KME21B2898, KME21D1652, KME21D1878, KME21D2020, KME21D2929, KME21D2935, KME21E0001, KME21E0002, KME21F0239, KME21F0434, KME21F1379, KME21F1887, KME21F2153, KME21G0013, KME21G0662, KME21G1616, KME21G1663, KME21G1923, KME21G1957, KME21G2511, KME21H0975, KME21H1183, KME21H1265, KME21J0157, KME21J0238, KME21J0497, KME21J0639, KME21J0756, KME21J0774, KME21J0855, KME21J1012, KME21J1207, KME21J1256, KME21J1540, KME21J1605, KME21J1885, KME21J2157, KME21K0003, KME21K0201, KME21K0241, KME21K0388, KME21K0635, KME21K0931, KME21K1129, KME21K1202, KME21K1334, KME21K1415, KME21K1557, KME21K1618, KME21K1816, KME21K2169, KME21K2270, KME21K2533, KME21K2746, KME21K3010, KME21L1055, KME21L1187, KME21L1279, KME21L1367, KME21L1930, KME21M0850, KME21M1390, KME21M1611, KME21M1634, KME21M1698, KME21M1726, KME21M1746, KME21M1864, KME21M1909, KME21M2007, KME21M2032, KME21M2072, KME21M2116, KME21M2147, KME21M2321, KME21M2363, KME21M2700, KME21M2727, KME21M2732, KME21M2744, KME21M3138, KME21M3224, KME21M3225, KME21M3274, KME22A0046, KME22A0224, KME22A0247, KME22A0356, KME22A0429, KME22A0513, KME22A0552, KME22A0621, KME22A0991, KME22A0992, KME22A1045, KME22A1133, KME22A2963, KME22A3194, KME22B0630, KME22B1947, KME22B2203, KME22B2316, KME22B2410, KME22B2585, KME22C1342, KME22C2121, KME22C2755, KME22C2854, KME22C3272, KME22D0480, KME22D1175, KME22D1826, KME22D2302, KME22D2405, KME22D3021, KME22D3274, KME22D3673, KME22D3674, KME22E0177, KME22E0317, KME22E0640, KME22E0655, KME22E0980, KME22E1974, KME22E2559, KME22E2560, KME22E2809, KME22E2919, KME22F0279, KME22F0523, KME22F0792, KME22F0870, KME22F2117, KME22F2905, KME22G0787, KME22G0800, KME22G0809, KME22G1036, KME22J1685, KME22J3142, KME22J3155, KME22J3259, KME22J3276, KME22J3403, KME22K0407, KME22K0509, KME22K2064, KME22K2267. A RECORDED FDA enforcement action (occurred=true).",
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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."
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      "name": "FDA classified recall Z-1888-2023 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.",
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      "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."
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      "@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.",
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      "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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