{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Miami Lakes",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87604",
      "recalling_firm": "Heartware, Inc.",
      "address_1": "14400 Nw 60th Ave",
      "address_2": "N/A",
      "postal_code": "33014-2807",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution and the countries of Italy, Great Britain, Germany, Japan.",
      "recall_number": "Z-1438-2021",
      "product_description": "Instructions for Use and Patient Manual for HeartWare HVAD System.  Accompanies these devices:  Heartware HVAD pump implant kits Models 1100, 1101, 1102, 1103, 1104, 1104JP, 1205, and MCS1705PU.      Heartware HVAD controller kits Models 1403US, 1407AU, 1407CA, 1407CH, 1407DE, 1407GB, 1407IL, 1407IN, 1407IT, 1407JP, 1407KR, 1420, and 1420JP.      Heartware HVAD controller AC adapter  Models 1430AR, 1430AU, 1430CA, 1430CH, 1430DE, 1430GB, 1430IL, 1430IN, 1430IT, 1430JP, and 1430US.      Heartware HVAD controller DC Adapter Model 1440.      Heartware HVAD data cable - monitor Model 1575.      Heartware HVAD battery pack Models 1650, 1650CA-CLIN, and 1650DE.      Heartware HVAD patient pack Model 1475.      Heartware HVAD waist pack Models 2050, 2050IL, and 2050US.      Heartware HVAD shoulder pack Models 2060, 2060IL, and 2060US.",
      "product_quantity": "23123 (11292 US)",
      "reason_for_recall": "IFU and Patient Manual updated to describe HVAD Controller Connection Verification. The labeling is being corrected to reflect the actual verified behavior of a successful connector to the controller, which is a \"beep\" and not \"audible click\", to clarify under what alarm conditions a beep will not be heard, and identify alternate confirmation methods (visual indicator) for successful connection.  NOTE: this update is included in the February 2021 Urgent Medical Device Notice also covered in recalls 87456 and 87603",
      "recall_initiation_date": "20210226",
      "center_classification_date": "20210420",
      "report_date": "20210428",
      "code_info": "Model, GTIN:   1100,  No GTIN Available;  1101,  No GTIN Available;  1102,  No GTIN Available;  1103,  00888707000017;  1104,  No GTIN Available;  1104JP,  00888707000697;  1205,  No GTIN Available;  MCS1705PU,  00888707005364;  1403US,  00888707000475;  1407AU,  00888707001663;  1407CA,  00888707002851;  1407CH,  00888707001694;  1407DE,  00888707001700;  1407GB,  00888707001717;  1407IL,  00888707001724;  1407IN,  00888707001731;  1407IT,  00888707001748;  1407JP,  00888707001755;  1407KR,  00888707001762;  1420,  00888707000420;  1420JP,  00888707000437;  1430AR,  00888707000826;  1430AU,  00888707000833;  1430CA,  00888707000857;  1430CH,  00888707000871;  1430DE,  00888707000864;  1430GB,  00888707000888;  1430IL,  00888707000901;  1430IN,  00888707000505;  1430IT,  00888707000895;  1430JP,  00888707000918;  1430US,  00888707000307;  1440,  00888707001885;  1575,  00888707008051;  1650,  00888707000376;  1650CA-CLIN,  00888707001588;  1650DE,  00888707001373;  1475,  00888707008037;  2050,  00888707008082;  2050IL,  00888707001410;  2050US,  00888707000048;  2060,  00888707008099;  2060IL,  00888707001427;  2060US,  00888707000055;",
      "more_code_info": ""
    }
  ]
}