{
  "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": [
    {
      "status": "Terminated",
      "city": "Waukesha",
      "state": "WI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88601",
      "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": "Visit",
      "distribution_pattern": "Domestic Distribution Only",
      "recall_number": "Z-2590-2021",
      "product_description": "AMX Navigate  Mobile X-Ray System",
      "product_quantity": "3 units",
      "reason_for_recall": "An unexpected column motion while attempting to park the column on the AMX Navigate mobile X-ray system.",
      "recall_initiation_date": "20210624",
      "center_classification_date": "20210929",
      "termination_date": "20230614",
      "report_date": "20211006",
      "code_info": "AMXNV2000001WK, AMXNV2000002WK, DF2401600003WK"
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}