{
  "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": "Waukesha",
      "state": "WI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72892",
      "recalling_firm": "GE Medical Systems, LLC",
      "address_1": "3200 N Grandview Blvd",
      "address_2": "N/A",
      "postal_code": "53188-1693",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Worldwide Distribution- US Distribution including the states of AZ, CA, CO, IL IN, MI, MN, NY, OH, OK, SD, TX, WI, VA, DE, FL, MD, ME, MO, NC, NH, OR, PA, TN, WI, DC, PR  and the countries of CANADA, CHINA, CZECH REPUBLIC, ITALY, JAPAN, NETHERLANDS, NEW ZEALAND, PORTUGAL, ROMANIA, SOUTH AFRICA, SWITZERLAND, TURKEY, SWEDEN, AUSTRALIA, BRAZIL, CZECH REPUBLIC, EGYPT, FRANCE, GERMANY, ITALY, MEXICO, RUSSIA, SAUDI ARABIA, TAIWAN, UNITED KINGDOM,  INDONESIA, ESTONIA, REPUBLIC OF KOREA,  POLAND, KUWAIT, SPAIN.",
      "recall_number": "Z-0201-2019",
      "product_description": "GE Healthcare, Discovery 3.0T MR750, 5148810-2, 5373011-2, 5499460-2.",
      "product_quantity": "356 (98 US; 258 OUS)",
      "reason_for_recall": "GE Healthcare has recently become aware of a potential safety issue with the 3.0T 6 Channel Flex Coil used with the 3T MR750W Surgical Suite Scanners.    Coil overheating can occur when the device is used in Mode 2 setup. This could lead to a serious patient thermal injury. There have been no injuries reported as a result of this issue.    UPDATE 5/27/2016:  Recall has been updated to include an additional product which includes the  Discovery 3.0T MR750 systems running Application Software DV24 R01, DV25 R02, or DV25.1 M3.",
      "recall_initiation_date": "20151207",
      "center_classification_date": "20181022",
      "termination_date": "20181108",
      "report_date": "20181031",
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}