{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Gainesville",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "74064",
      "recalling_firm": "Invivo Corporation",
      "address_1": "3545 SW 47th Ave",
      "address_2": "N/A",
      "postal_code": "32608-7691",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "WI",
      "recall_number": "Z-2688-2016",
      "product_description": "Invivo Sentinelle Venguard Breast MRI Auxiliary Table/Tabletop with 8/16 Channel Coil Array for GE 1.5T/3T MRI Systems.",
      "product_quantity": "3",
      "reason_for_recall": "A diode was inadvertently not assembled  into the system, which may result in coil overheating",
      "recall_initiation_date": "20160506",
      "center_classification_date": "20160830",
      "termination_date": "20190821",
      "report_date": "20160907",
      "code_info": "Model #: 9896-032-14382; Serial #: 13 (production order 301128446), 14 (production order 301153586), and 15 (production order 301153587)."
    }
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}