{
  "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": "2026-09-05",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "cfres_id": "154236",
      "product_res_number": "Z-1832-2017",
      "event_date_initiated": "2017-03-10",
      "event_date_created": "2017-04-25",
      "recall_status": "Open, Classified",
      "res_event_number": "76807",
      "product_code": "DSQ",
      "pma_numbers": [
        "P100047"
      ],
      "product_description": "HeartWare Ventricular Assist System (HVAD) Pump Driveline Splice Kit \n\nProduct Usage:\nIs intended to repair the driveline cable once an electrical break has been identified. These repairs are limited to the portion of the driveline that is outside the patient boundary (exit side).",
      "code_info": "Product Codes: ASY00116 and ASY00281 Serial # All patients with Drivelines splice repair performed prior April 2015",
      "firm_fei_number": "3007042319",
      "recalling_firm": "Heartware",
      "address_1": "14400 NW 60th Ave",
      "city": "Miami Lakes",
      "state": "FL",
      "postal_code": "33014-2807",
      "additional_info_contact": "305-364-1575",
      "reason_for_recall": "In April 2015, HeartWare, now a part of Medtronic, notified users of a safety issue related to the HVAD Pump Driveline Splice Kit. Medtronic now intends to send a follow-up communication to identified clinicians informing them that a new, improved splice kit is available.",
      "root_cause_description": "Device Design",
      "action": "HeartWare, now a part of Medtronic sent an Urgent Medical Device Recall letter on April 2015 and a follow-up letter on March 2017, to customers via overnight mail and/or email..  The letters identified the affected product, problem and actions to be taken.  Customers were instructed to review the recall notice, forward the notice to individuals within their organization who need to be aware of the notice, complete, sign, and return the Acknowledgement Form . For questions contact your local HeartWare representative.",
      "product_quantity": "9 units",
      "distribution_pattern": "Worldwide Distribution - US Nationwide in the states of FL, MO, TN, KY, NY and the country of Germany.",
      "openfda": {
        "device_name": "Ventricular (Assist) Bypass",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3",
        "pma_number": [
          "P920014",
          "P980012",
          "P160054",
          "P160035",
          "P900023",
          "P100047",
          "P170038",
          "P060040",
          "P870072"
        ],
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}