{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Miami Lakes",
      "address_1": "14400 Nw 60th Ave",
      "reason_for_recall": "The pump has an impeller with a shroud height that did not meet the lower control limit.",
      "address_2": "",
      "product_quantity": "1 unit",
      "code_info": "UDI: 00888707007139. Serial Number HW42843",
      "center_classification_date": "20210713",
      "distribution_pattern": "International distribution to the country of Germany.",
      "state": "FL",
      "product_description": "HeartWare, HVAD Pump Implant Kit, REF MCS1705PU - Product Usage: indicated for hemodynamic support in patients with advanced, refractory left ventricular heart failure; either as a Bridge to Cardiac Transplantation (BTT), myocardial recovery, or as Destination Therapy (DT) in patients for whom subsequent transplantation is not planned.",
      "report_date": "20210721",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Heartware, Inc.",
      "recall_number": "Z-2072-2021",
      "initial_firm_notification": "Telephone",
      "product_type": "Devices",
      "event_id": "88135",
      "more_code_info": "",
      "recall_initiation_date": "20210528",
      "postal_code": "33014-2807",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}