{
  "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": "New York",
      "address_1": "333 W 52nd St Fl 15",
      "reason_for_recall": "There is a potential for the male connectors on external cables to become damaged. This could include a detached male connector housing, misaligned connector, cracked connector housing, and bent pins.",
      "address_2": "",
      "product_quantity": "274",
      "code_info": "All systems/cables",
      "center_classification_date": "20181218",
      "distribution_pattern": "Products were distributed to the following US states:  FL, NY, and UT.    Products were distributed to the following foreign countries:  Croatia, Czech Republic, France, Hungary, India, Italy, and Japan.",
      "state": "NY",
      "product_description": "Jarvik 2000 Ventricular Assist System external components:  JHI-212 Y Cable, JHI-202 Lithium-ion Battery Cable, JHI-204 Extensions Cable, JHI-201 Pedestal Cable",
      "report_date": "20181226",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Jarvik Heart Inc",
      "recall_number": "Z-0629-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "81709",
      "termination_date": "20200501",
      "more_code_info": "",
      "recall_initiation_date": "20181015",
      "postal_code": "10019-6238",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}