{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Buc",
      "state": "",
      "country": "France",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93837",
      "recalling_firm": "GE Medical Systems, SCS",
      "address_1": "283 rue de la Miniere",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Us Nationwide-Worldwide Distribution",
      "recall_number": "Z-0862-2024",
      "product_description": "Senographe Pristina",
      "product_quantity": "180 units (60 US; 120 OUS)",
      "reason_for_recall": "X-ray exposure termination audible signal on Senographe Pristina with Efficiency Suite 2 intermittently not emitted per 21CFR 1020.31(j) requirements.",
      "recall_initiation_date": "20231226",
      "center_classification_date": "20240208",
      "report_date": "20240214",
      "code_info": "GTIN(s): 195278022745, 195278276971, 195278628916, 195278661999, 195278665379, 840682118460, 840682142052, 840682145879",
      "more_code_info": ""
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}