{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Waukesha",
      "state": "WI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90587",
      "recalling_firm": "GE Healthcare, LLC",
      "address_1": "3000 N Grandview Blvd",
      "address_2": "N/A",
      "postal_code": "53188-1615",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution in the states of AL, AZ, CA, MI, MN, NY, and WI.  There was government distribution but no military distribution. The countries of China, France, Hong Kong, India, Italy, Japan, Korea, Kuwait, Norway, Oman, Saudi Arabia, Slovakia, Spain, Sweden, Switzerland, Thailand, Turkey, and United Kingdom.",
      "recall_number": "Z-1430-2022",
      "product_description": "SIGNA Premier magnetic resonance scanner, model 5748519.",
      "product_quantity": "52",
      "reason_for_recall": "Under rare conditions, SIGNA Premier gradient coils could result in elevated acoustic noise during scanning.  After prolonged periods of elevated acoustic noise, this could potentially lead to hearing loss.",
      "recall_initiation_date": "20220624",
      "center_classification_date": "20220721",
      "report_date": "20220727",
      "code_info": "SIGNA Premier GTINs:  00840682135269 and 00195278010797"
    }
  ]
}