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  "name": "SENSATION PLUS 7.5Fr IAB, Intra-Aortic Balloon Catheter and Accessories, used to provide counter pulsation therapy in the aorta    Product Description                                                                                            Part Number  SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES\tD684-00-0568-01  SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES (W/O STATLOCK)\tD684-00-0568-03  SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES (WITH PRESSURE \tD684-00-0568-05  SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES (TURKEY)\tD684-00-0568-09  SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES, US ONLY\tD684-00-0568-01U  PACKAGED INSERTION KIT - SENSATION PLUS 7.5 Fr. 40 cc IAB  D884-00-0019-22",
  "description": "FDA recall Z-2221-2023 — Datascope Corp. is recalling SENSATION PLUS 7.5Fr IAB, Intra-Aortic Balloon Catheter and Accessories, used to provide counter pulsation therapy in the aorta    Product Description                                                                                            Part Number  SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES\tD684-00-0568-01  SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES (W/O STATLOCK)\tD684-00-0568-03  SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES (WITH PRESSURE \tD684-00-0568-05  SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES (TURKEY)\tD684-00-0568-09  SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES, US ONLY\tD684-00-0568-01U  PACKAGED INSERTION KIT - SENSATION PLUS 7.5 Fr. 40 cc IAB  D884-00-0019-22 (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",
  "isBasedOn": {
    "@type": "schema:Dataset",
    "name": "openFDA drug & device enforcement (recall) reports",
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      "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-2221-2023&lang=eng",
  "about": {
    "@type": "schema:MedicalDevice",
    "name": "SENSATION PLUS 7.5Fr IAB, Intra-Aortic Balloon Catheter and Accessories, used to provide counter pulsation therapy in the aorta    Product Description                                                                                            Part Number  SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES\tD684-00-0568-01  SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES (W/O STATLOCK)\tD684-00-0568-03  SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES (WITH PRESSURE \tD684-00-0568-05  SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES (TURKEY)\tD684-00-0568-09  SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES, US ONLY\tD684-00-0568-01U  PACKAGED INSERTION KIT - SENSATION PLUS 7.5 Fr. 40 cc IAB  D884-00-0019-22",
    "manufacturer": {
      "@type": "schema:Organization",
      "name": "Datascope Corp."
    }
  },
  "claims": [
    {
      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-2221-2023/enforcement-record",
      "@type": "schema:Claim",
      "name": "FDA recall Z-2221-2023: Datascope Corp. is recalling SENSATION PLUS 7.5Fr IAB, Intra-Aortic Balloon Catheter and Accessories, used to provide counter pulsation therapy in the aorta    Product Description                                                                                            Part Number  SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES\tD684-00-0568-01  SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES (W/O STATLOCK)\tD684-00-0568-03  SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES (WITH PRESSURE \tD684-00-0568-05  SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES (TURKEY)\tD684-00-0568-09  SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES, US ONLY\tD684-00-0568-01U  PACKAGED INSERTION KIT - SENSATION PLUS 7.5 Fr. 40 cc IAB  D884-00-0019-22",
      "text": "The FDA logged enforcement record Z-2221-2023: Datascope Corp. is voluntarily recalling SENSATION PLUS 7.5Fr IAB, Intra-Aortic Balloon Catheter and Accessories, used to provide counter pulsation therapy in the aorta    Product Description                                                                                            Part Number  SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES\tD684-00-0568-01  SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES (W/O STATLOCK)\tD684-00-0568-03  SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES (WITH PRESSURE \tD684-00-0568-05  SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES (TURKEY)\tD684-00-0568-09  SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES, US ONLY\tD684-00-0568-01U  PACKAGED INSERTION KIT - SENSATION PLUS 7.5 Fr. 40 cc IAB  D884-00-0019-22 — reason: During IAB catheter insertion, the introducer dilator may fracture at the hub, leaving the body of the introducer dilator housed within the sheath.  Risks to health include damage to the femoral artery, descending aorta, or embolization; surgical intervention and delay of IAB therapy may also result. Firm has received 10 complaints, including 3 serious adverse events and 1 patient death.. Status: Ongoing — the recall is still being carried out.. Initiated 2023-06-23. Affected lots/codes: Product Description                                                    UDI SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES 10607567108063 SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES (W/O STATLOCK) 10607567109428 SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES (WITH PRESSURE  10607567109442 SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES (TURKEY) 10607567113166 SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES, US ONLY 10607567109565 PACKAGED INSERTION KIT - SENSATION PLUS 7.5 Fr. 40 cc IAB   10607567108612. A RECORDED FDA enforcement action (occurred=true).",
      "claimType": "official_fact",
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        "supported": true,
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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-2221-2023&lang=eng",
        "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-2221-2023&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-2221-2023/fda-classification",
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      "name": "FDA classified recall Z-2221-2023 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.",
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        "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-2221-2023&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-2221-2023/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",
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        "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-2221-2023",
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            "Value": "Z-2221-2023",
            "Status": "recorded"
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            "Value": "Devices",
            "Status": "recorded"
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            "Field": "Classification",
            "Value": "Class II",
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            "Value": "Ongoing — the recall is still being carried out.",
            "Status": "recorded"
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          "position": 5,
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            "Field": "Recalling firm",
            "Value": "Datascope Corp.",
            "Status": "recorded"
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          "item": {
            "Field": "Reason",
            "Value": "During IAB catheter insertion, the introducer dilator may fracture at the hub, leaving the body of the introducer dilator housed within the sheath.  Risks to health include damage to the femoral artery, descending aorta, or embolization; surgical intervention and delay of IAB therapy may also result. Firm has received 10 complaints, including 3 serious adverse events and 1 patient death.",
            "Status": "recorded"
          }
        },
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          "@type": "schema:ListItem",
          "position": 7,
          "item": {
            "Field": "Initiated",
            "Value": "2023-06-23",
            "Status": "recorded"
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          "position": 8,
          "item": {
            "Field": "Lot/code info",
            "Value": "Product Description                                                    UDI SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES 10607567108063 SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES (W/O STATLOCK) 10607567109428 SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES (WITH PRESSURE  10607567109442 SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES (TURKEY) 10607567113166 SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES, US ONLY 10607567109565 PACKAGED INSERTION KIT - SENSATION PLUS 7.5 Fr. 40 cc IAB   10607567108612",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 9,
          "item": {
            "Field": "Distribution pattern",
            "Value": "Domestic distribution nationwide. International distribution worldwide.",
            "Status": "recorded"
          }
        }
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}