{
  "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": "Waukesha",
      "address_1": "3000 N Grandview Blvd",
      "reason_for_recall": "GE Healthcare has recently become aware of an issue on the affected products listed below where the \"Patient Orientation\" button may inadvertently be clicked when intending to click on the \"Save RX\" button.  This changes the prescribed patient orientation on the system prior to running the initial 3-Plane Localizer Scan (See Figure 1 for reference to buttons.)  Selecting and saving a patient orientation that does not match the patient's actual position may result in incorrectly annotated and/or flipped images.",
      "address_2": "",
      "product_quantity": "242 units",
      "code_info": "",
      "center_classification_date": "20210712",
      "distribution_pattern": "Worldwide distributions.",
      "state": "WI",
      "product_description": "SIGNA MR355, SIGNA MR360, Nuclear Magnetic Resonance Imaging System",
      "report_date": "20210721",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "GE Healthcare, LLC",
      "recall_number": "Z-2059-2021",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "88147",
      "more_code_info": "",
      "recall_initiation_date": "20210604",
      "postal_code": "53188-1615",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}