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  "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-0414-2024.jsonld",
  "@type": "schema:Dataset",
  "name": "TruWave with Vamp System Pressure monitoring set,   REF: PXAVMP(3cc)/VAMP 68 in (173cm)  PXAVMP3: x3 (3cc)/VAMP  PXVK0364:(3cc)/VAMP 96in (241cm);  PXVK0853: x3 (3cc)/VAMP 76in (193cm);  PXVK0996:(3cc)/VAMP 68in (174cm);  PXVMP2X21: x2 (3cc)/VAMP;  PXVMP2X22: x2 (3cc)/VAMP 63 in (160cm);  PXVMP3X32: x3 (3cc)/VAMP 75in (190cm);  PXVP0041: (3cc)/VAMP Plus 96in (244cm);  PXVP0550: x3 (3cc)/VAMP Plus 91 in (231cm);  PXVP1071: x3 (3cc)/VAMP Plus 87in (221cm);  PXVP1087: x4(3cc)/VAMP Plus;  PXVP2260: (3cc)/VAMP Plus 60in (150cm);  PXVP2272: (3cc)/VAMP Plus 72in (180cm);  PXVP2284: (3cc)/VAMP Plus 84in (210cm);  PXVP2284AT3: (3cc)/VAMP Plus 84in (210cm);  PXVP23X3: x3: (3cc)/VAMP Plus;  PXVP23X3AT3: x3 (3cc)/VAMP Plus;  PXVP2X2AT3: x2 (3cc)/VAMP Plus;  PXVPL0111: (3cc)/VAMP Plus 84in (213cm);  PXVMP160: 3cc/VAMP 60 in (150cm);  PXVMP172: 3cc/VAMP 72in)180cm);  PXVMP184:3cc/VAMP 84in (210cm);  PXVMP260:3cc/VAMP 60in (150cm);  PXVFL10017: (3cc)/VAMP Flex 83in (210cm);  PXVP0034: (3cc)/VAMP Plus 87in (220cm);  T001691A: (3cc)/VAMP Plus;  T001691M: (3cc)/VAMP Plus (215cm);  T001744M:(3cc)/VAMP 93in (236 cm);  T100671M: x3(3cc)/VAMP Plus (215cm);  T001760A :x2(3cc)/VAMP Plus;  T001765A: (3cc)/60in (150cm);  T005021M: (3cc)/VAMP Flex (195cm);  T005089M: x2 (3cc)/VAMP Flex (195 cm) ;  T005091M: x3(3cc)/VAMP Flex (195cm);  T434501B: x2(3cc)/VAMP 88in (225cm);  T440B26B: x2 (3cc)/VAMP 88in (225cm);  T450545A: x3 (3cc)/VAMP 75in (190cm);  T460241A: (3cc)/VAMP Plus 69in (175cm);  T530219D: x2 (3cc)/VAMP Plus 65in (165cm)",
  "description": "FDA recall Z-0414-2024 — Edwards Lifesciences, LLC is recalling TruWave with Vamp System Pressure monitoring set,   REF: PXAVMP(3cc)/VAMP 68 in (173cm)  PXAVMP3: x3 (3cc)/VAMP  PXVK0364:(3cc)/VAMP 96in (241cm);  PXVK0853: x3 (3cc)/VAMP 76in (193cm);  PXVK0996:(3cc)/VAMP 68in (174cm);  PXVMP2X21: x2 (3cc)/VAMP;  PXVMP2X22: x2 (3cc)/VAMP 63 in (160cm);  PXVMP3X32: x3 (3cc)/VAMP 75in (190cm);  PXVP0041: (3cc)/VAMP Plus 96in (244cm);  PXVP0550: x3 (3cc)/VAMP Plus 91 in (231cm);  PXVP1071: x3 (3cc)/VAMP Plus 87in (221cm);  PXVP1087: x4(3cc)/VAMP Plus;  PXVP2260: (3cc)/VAMP Plus 60in (150cm);  PXVP2272: (3cc)/VAMP Plus 72in (180cm);  PXVP2284: (3cc)/VAMP Plus 84in (210cm);  PXVP2284AT3: (3cc)/VAMP Plus 84in (210cm);  PXVP23X3: x3: (3cc)/VAMP Plus;  PXVP23X3AT3: x3 (3cc)/VAMP Plus;  PXVP2X2AT3: x2 (3cc)/VAMP Plus;  PXVPL0111: (3cc)/VAMP Plus 84in (213cm);  PXVMP160: 3cc/VAMP 60 in (150cm);  PXVMP172: 3cc/VAMP 72in)180cm);  PXVMP184:3cc/VAMP 84in (210cm);  PXVMP260:3cc/VAMP 60in (150cm);  PXVFL10017: (3cc)/VAMP Flex 83in (210cm);  PXVP0034: (3cc)/VAMP Plus 87in (220cm);  T001691A: (3cc)/VAMP Plus;  T001691M: (3cc)/VAMP Plus (215cm);  T001744M:(3cc)/VAMP 93in (236 cm);  T100671M: x3(3cc)/VAMP Plus (215cm);  T001760A :x2(3cc)/VAMP Plus;  T001765A: (3cc)/60in (150cm);  T005021M: (3cc)/VAMP Flex (195cm);  T005089M: x2 (3cc)/VAMP Flex (195 cm) ;  T005091M: x3(3cc)/VAMP Flex (195cm);  T434501B: x2(3cc)/VAMP 88in (225cm);  T440B26B: x2 (3cc)/VAMP 88in (225cm);  T450545A: x3 (3cc)/VAMP 75in (190cm);  T460241A: (3cc)/VAMP Plus 69in (175cm);  T530219D: x2 (3cc)/VAMP Plus 65in (165cm) (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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    "@type": "schema:MedicalDevice",
    "name": "TruWave with Vamp System Pressure monitoring set,   REF: PXAVMP(3cc)/VAMP 68 in (173cm)  PXAVMP3: x3 (3cc)/VAMP  PXVK0364:(3cc)/VAMP 96in (241cm);  PXVK0853: x3 (3cc)/VAMP 76in (193cm);  PXVK0996:(3cc)/VAMP 68in (174cm);  PXVMP2X21: x2 (3cc)/VAMP;  PXVMP2X22: x2 (3cc)/VAMP 63 in (160cm);  PXVMP3X32: x3 (3cc)/VAMP 75in (190cm);  PXVP0041: (3cc)/VAMP Plus 96in (244cm);  PXVP0550: x3 (3cc)/VAMP Plus 91 in (231cm);  PXVP1071: x3 (3cc)/VAMP Plus 87in (221cm);  PXVP1087: x4(3cc)/VAMP Plus;  PXVP2260: (3cc)/VAMP Plus 60in (150cm);  PXVP2272: (3cc)/VAMP Plus 72in (180cm);  PXVP2284: (3cc)/VAMP Plus 84in (210cm);  PXVP2284AT3: (3cc)/VAMP Plus 84in (210cm);  PXVP23X3: x3: (3cc)/VAMP Plus;  PXVP23X3AT3: x3 (3cc)/VAMP Plus;  PXVP2X2AT3: x2 (3cc)/VAMP Plus;  PXVPL0111: (3cc)/VAMP Plus 84in (213cm);  PXVMP160: 3cc/VAMP 60 in (150cm);  PXVMP172: 3cc/VAMP 72in)180cm);  PXVMP184:3cc/VAMP 84in (210cm);  PXVMP260:3cc/VAMP 60in (150cm);  PXVFL10017: (3cc)/VAMP Flex 83in (210cm);  PXVP0034: (3cc)/VAMP Plus 87in (220cm);  T001691A: (3cc)/VAMP Plus;  T001691M: (3cc)/VAMP Plus (215cm);  T001744M:(3cc)/VAMP 93in (236 cm);  T100671M: x3(3cc)/VAMP Plus (215cm);  T001760A :x2(3cc)/VAMP Plus;  T001765A: (3cc)/60in (150cm);  T005021M: (3cc)/VAMP Flex (195cm);  T005089M: x2 (3cc)/VAMP Flex (195 cm) ;  T005091M: x3(3cc)/VAMP Flex (195cm);  T434501B: x2(3cc)/VAMP 88in (225cm);  T440B26B: x2 (3cc)/VAMP 88in (225cm);  T450545A: x3 (3cc)/VAMP 75in (190cm);  T460241A: (3cc)/VAMP Plus 69in (175cm);  T530219D: x2 (3cc)/VAMP Plus 65in (165cm)",
    "manufacturer": {
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      "name": "Edwards Lifesciences, LLC"
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    {
      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-0414-2024/enforcement-record",
      "@type": "schema:Claim",
      "name": "FDA recall Z-0414-2024: Edwards Lifesciences, LLC is recalling TruWave with Vamp System Pressure monitoring set,   REF: PXAVMP(3cc)/VAMP 68 in (173cm)  PXAVMP3: x3 (3cc)/VAMP  PXVK0364:(3cc)/VAMP 96in (241cm);  PXVK0853: x3 (3cc)/VAMP 76in (193cm);  PXVK0996:(3cc)/VAMP 68in (174cm);  PXVMP2X21: x2 (3cc)/VAMP;  PXVMP2X22: x2 (3cc)/VAMP 63 in (160cm);  PXVMP3X32: x3 (3cc)/VAMP 75in (190cm);  PXVP0041: (3cc)/VAMP Plus 96in (244cm);  PXVP0550: x3 (3cc)/VAMP Plus 91 in (231cm);  PXVP1071: x3 (3cc)/VAMP Plus 87in (221cm);  PXVP1087: x4(3cc)/VAMP Plus;  PXVP2260: (3cc)/VAMP Plus 60in (150cm);  PXVP2272: (3cc)/VAMP Plus 72in (180cm);  PXVP2284: (3cc)/VAMP Plus 84in (210cm);  PXVP2284AT3: (3cc)/VAMP Plus 84in (210cm);  PXVP23X3: x3: (3cc)/VAMP Plus;  PXVP23X3AT3: x3 (3cc)/VAMP Plus;  PXVP2X2AT3: x2 (3cc)/VAMP Plus;  PXVPL0111: (3cc)/VAMP Plus 84in (213cm);  PXVMP160: 3cc/VAMP 60 in (150cm);  PXVMP172: 3cc/VAMP 72in)180cm);  PXVMP184:3cc/VAMP 84in (210cm);  PXVMP260:3cc/VAMP 60in (150cm);  PXVFL10017: (3cc)/VAMP Flex 83in (210cm);  PXVP0034: (3cc)/VAMP Plus 87in (220cm);  T001691A: (3cc)/VAMP Plus;  T001691M: (3cc)/VAMP Plus (215cm);  T001744M:(3cc)/VAMP 93in (236 cm);  T100671M: x3(3cc)/VAMP Plus (215cm);  T001760A :x2(3cc)/VAMP Plus;  T001765A: (3cc)/60in (150cm);  T005021M: (3cc)/VAMP Flex (195cm);  T005089M: x2 (3cc)/VAMP Flex (195 cm) ;  T005091M: x3(3cc)/VAMP Flex (195cm);  T434501B: x2(3cc)/VAMP 88in (225cm);  T440B26B: x2 (3cc)/VAMP 88in (225cm);  T450545A: x3 (3cc)/VAMP 75in (190cm);  T460241A: (3cc)/VAMP Plus 69in (175cm);  T530219D: x2 (3cc)/VAMP Plus 65in (165cm)",
      "text": "The FDA logged enforcement record Z-0414-2024: Edwards Lifesciences, LLC is voluntarily recalling TruWave with Vamp System Pressure monitoring set,   REF: PXAVMP(3cc)/VAMP 68 in (173cm)  PXAVMP3: x3 (3cc)/VAMP  PXVK0364:(3cc)/VAMP 96in (241cm);  PXVK0853: x3 (3cc)/VAMP 76in (193cm);  PXVK0996:(3cc)/VAMP 68in (174cm);  PXVMP2X21: x2 (3cc)/VAMP;  PXVMP2X22: x2 (3cc)/VAMP 63 in (160cm);  PXVMP3X32: x3 (3cc)/VAMP 75in (190cm);  PXVP0041: (3cc)/VAMP Plus 96in (244cm);  PXVP0550: x3 (3cc)/VAMP Plus 91 in (231cm);  PXVP1071: x3 (3cc)/VAMP Plus 87in (221cm);  PXVP1087: x4(3cc)/VAMP Plus;  PXVP2260: (3cc)/VAMP Plus 60in (150cm);  PXVP2272: (3cc)/VAMP Plus 72in (180cm);  PXVP2284: (3cc)/VAMP Plus 84in (210cm);  PXVP2284AT3: (3cc)/VAMP Plus 84in (210cm);  PXVP23X3: x3: (3cc)/VAMP Plus;  PXVP23X3AT3: x3 (3cc)/VAMP Plus;  PXVP2X2AT3: x2 (3cc)/VAMP Plus;  PXVPL0111: (3cc)/VAMP Plus 84in (213cm);  PXVMP160: 3cc/VAMP 60 in (150cm);  PXVMP172: 3cc/VAMP 72in)180cm);  PXVMP184:3cc/VAMP 84in (210cm);  PXVMP260:3cc/VAMP 60in (150cm);  PXVFL10017: (3cc)/VAMP Flex 83in (210cm);  PXVP0034: (3cc)/VAMP Plus 87in (220cm);  T001691A: (3cc)/VAMP Plus;  T001691M: (3cc)/VAMP Plus (215cm);  T001744M:(3cc)/VAMP 93in (236 cm);  T100671M: x3(3cc)/VAMP Plus (215cm);  T001760A :x2(3cc)/VAMP Plus;  T001765A: (3cc)/60in (150cm);  T005021M: (3cc)/VAMP Flex (195cm);  T005089M: x2 (3cc)/VAMP Flex (195 cm) ;  T005091M: x3(3cc)/VAMP Flex (195cm);  T434501B: x2(3cc)/VAMP 88in (225cm);  T440B26B: x2 (3cc)/VAMP 88in (225cm);  T450545A: x3 (3cc)/VAMP 75in (190cm);  T460241A: (3cc)/VAMP Plus 69in (175cm);  T530219D: x2 (3cc)/VAMP Plus 65in (165cm) — reason: Their is the potential for flushing difficulties during setup of the pressure monitoring kit with pressure transducer.. Status: Ongoing — the recall is still being carried out.. Initiated 2023-10-04. Affected lots/codes: PXAVMP:UDI: 00690103011494/Lot # 64817849; PXAVMP3: UDI:07460691950085/Lot # 64918575; PXVK0364:UDI:07460691954526/Lot # 64858007; PXVK0853: UDI: 07460691957671/Lot # 65060361; PXVK0996:UDI: 07460691955431/Lot # 64858275; PXVMP2X21:UDI: 07460691950115/Lot # 64992080; PXVMP2X22: UDI: 00690103016765/Lot # 64891427; PXVMP3X32:UDI: 0690103016802/Lot # 65008748; PXVP0041: UDI: 00690103197983/Lot # 64835537; PXVP0550:UDI: 07460691949911/Lot # 64818013, 64858077, 64891424, 64918588, 64985484; PXVP1071: UDI: 07460691955462/Lot # 64807998, 64807999; PXVP1087: UDI: 07460691957886/Lot # 65035078, 65079515; PXVP2260: UDI: 07460691950108/Lot # 64858071, 64858103, 64891419, 64906892; PXVP2272:UDI: 07460691950184/Lot # 64752261, 64906891, 65138017; PXVP2284: UDI: 07460691950177/Lot # 64818005, 64818008, 64818011, 64891421, 64933492, 64933493, 64964755, 64964759, 64964760, 64964761, 64998878, 65060446; PXVP2284AT3: UDI: 07460691950436/Lot # 64722680, 64858285, 64951434, 64980108, 64992088; PXVP23X3:UDI: 07460691950092/Lot # 64998879, 65060444; PXVP23X3AT3: UDI: 07460691950443/Lot # 64695848, 64779289, 64858072, 64858290, 64992092,65060447; PXVP2X2AT3: UDI:07460691950467/Lot # 64858075; PXVPL0111: UDI: 00690103200386/Lot # 64933462; PXVMP160: UDI:/Lot # 64779279, 64918578, 64933556, 64933559; PXVMP172: UDI:/Lot # 64835579; PXVMP184:UDI:/Lot # 64949045, 64983460, 65042811; PXVMP260:UDI:/Lot # 64629075, 64964750, 64980101; PXVFL10017:UDI:00690103210798/Lot # 64923241; PXVP0034:UDI:00690103197945/Lot # 64835538, 65019842; T001691A:UDI: 07460691947627/Lot # 64793360 64807977 64817834 64835567 64835568 65008739 65019862 65035054 65048943; T001744M:UDI: 07460691959507/Lot # 64526411, 64891383; T100671M:UDI: 07460691959491/Lot # 64912244; T001760A: UDI:07460691947566/ Lot # 65008764, 65019890, 65067580; T001765A: UDI:07460691947290/ Lot # 64891376, 64906871, 64980035, 64983290, 65035029; T005021M:UDI:07460691959538/ Lot # 64858230, 64923245; T005089M:UDI:07460691959545/Lot #64933442, 65060364 T005091M:UDI:07460691959552/Lot # 64807926 T434501B:UDI: 07460691956636/ Lot # 64817812 T440B26B:UDI:07460691949553/ Lot # 64817809, 64817936; T450545A:UDI: 07460691931572/ Lot # 65035081; T460241A: UDI:07460691949188/ Lot # 64933451; T530219D:UDI:07460691948259/ Lot # 65067546. A RECORDED FDA enforcement action (occurred=true).",
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      "commercialInfluence": false,
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        "value": "Devices recall, status Ongoing",
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          "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-0414-2024&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-0414-2024/fda-classification",
      "@type": "schema:Claim",
      "name": "FDA classified recall Z-0414-2024 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": {
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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-0414-2024&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-0414-2024&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-0414-2024/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-0414-2024",
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            "Value": "Z-0414-2024",
            "Status": "recorded"
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          "position": 2,
          "item": {
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            "Value": "Devices",
            "Status": "recorded"
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          "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": "Edwards Lifesciences, LLC",
            "Status": "recorded"
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          "item": {
            "Field": "Reason",
            "Value": "Their is the potential for flushing difficulties during setup of the pressure monitoring kit with pressure transducer.",
            "Status": "recorded"
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          "position": 7,
          "item": {
            "Field": "Initiated",
            "Value": "2023-10-04",
            "Status": "recorded"
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          "item": {
            "Field": "Lot/code info",
            "Value": "PXAVMP:UDI: 00690103011494/Lot # 64817849; PXAVMP3: UDI:07460691950085/Lot # 64918575; PXVK0364:UDI:07460691954526/Lot # 64858007; PXVK0853: UDI: 07460691957671/Lot # 65060361; PXVK0996:UDI: 07460691955431/Lot # 64858275; PXVMP2X21:UDI: 07460691950115/Lot # 64992080; PXVMP2X22: UDI: 00690103016765/Lot # 64891427; PXVMP3X32:UDI: 0690103016802/Lot # 65008748; PXVP0041: UDI: 00690103197983/Lot # 64835537; PXVP0550:UDI: 07460691949911/Lot # 64818013, 64858077, 64891424, 64918588, 64985484; PXVP1071: UDI: 07460691955462/Lot # 64807998, 64807999; PXVP1087: UDI: 07460691957886/Lot # 65035078, 65079515; PXVP2260: UDI: 07460691950108/Lot # 64858071, 64858103, 64891419, 64906892; PXVP2272:UDI: 07460691950184/Lot # 64752261, 64906891, 65138017; PXVP2284: UDI: 07460691950177/Lot # 64818005, 64818008, 64818011, 64891421, 64933492, 64933493, 64964755, 64964759, 64964760, 64964761, 64998878, 65060446; PXVP2284AT3: UDI: 07460691950436/Lot # 64722680, 64858285, 64951434, 64980108, 64992088; PXVP23X3:UDI: 07460691950092/Lot # 64998879, 65060444; PXVP23X3AT3: UDI: 07460691950443/Lot # 64695848, 64779289, 64858072, 64858290, 64992092,65060447; PXVP2X2AT3: UDI:07460691950467/Lot # 64858075; PXVPL0111: UDI: 00690103200386/Lot # 64933462; PXVMP160: UDI:/Lot # 64779279, 64918578, 64933556, 64933559; PXVMP172: UDI:/Lot # 64835579; PXVMP184:UDI:/Lot # 64949045, 64983460, 65042811; PXVMP260:UDI:/Lot # 64629075, 64964750, 64980101; PXVFL10017:UDI:00690103210798/Lot # 64923241; PXVP0034:UDI:00690103197945/Lot # 64835538, 65019842; T001691A:UDI: 07460691947627/Lot # 64793360 64807977 64817834 64835567 64835568 65008739 65019862 65035054 65048943; T001744M:UDI: 07460691959507/Lot # 64526411, 64891383; T100671M:UDI: 07460691959491/Lot # 64912244; T001760A: UDI:07460691947566/ Lot # 65008764, 65019890, 65067580; T001765A: UDI:07460691947290/ Lot # 64891376, 64906871, 64980035, 64983290, 65035029; T005021M:UDI:07460691959538/ Lot # 64858230, 64923245; T005089M:UDI:07460691959545/Lot #64933442, 65060364 T005091M:UDI:07460691959552/Lot # 64807926 T434501B:UDI: 07460691956636/ Lot # 64817812 T440B26B:UDI:07460691949553/ Lot # 64817809, 64817936; T450545A:UDI: 07460691931572/ Lot # 65035081; T460241A: UDI:07460691949188/ Lot # 64933451; T530219D:UDI:07460691948259/ Lot # 65067546",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 9,
          "item": {
            "Field": "Distribution pattern",
            "Value": "US: AK\tAL\tAR\tAZ\tCA\tCO\tCT\tDC\tDE\tFL\tGA\tHI\tIA\tID\tIL\tIN\tKS\tKY\tLA\tMA\tMD\tME\tMI\tMN\tMO\tMS\tMT\tNC\tND\tNE\tNH\tNJ\tNM\tNV\tNY\tOH\tOK\tOR\tPA\tPR\tRI\tSC\tSD\tTN\tTX\tUT\tVA\tWA\tWI\tWV\tWY  OUS: Argentina\tAustralia\tAustria\tBahrain\tBelgium\tBrazil\tCanada\tCANARY ISLANDS\tChile\tColombia\tCosta Rica\tCzech Republic\tDenmark\tEcuador\tFaroe Islands\tFrance\tGermany\tGreece\tGuatemala\tHong Kong\tIndonesia\tIreland\tIsrael\tItaly\tJapan\tMalaysia\tNetherlands\tNew Zealand\tNorthern Ireland\tNorway\tPanama\tPoland\tPortugal\tSaudi Arabia\tSingapore\tSlovakia\tSlovenia\tSouth Korea\tSpain\tSweden\tSwitzerland\tUnited Arab Emirates (UAE)\tUnited Kingdom\tVietnam",
            "Status": "recorded"
          }
        }
      ]
    }
  ]
}