{
  "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": "2026-04-22",
    "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": "62946",
      "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 -- USA (nationwide) Distribution",
      "recall_number": "Z-2256-2012",
      "product_description": "Optima XR200amx.  Mobile general purpose radiographic imaging of the human head and body.",
      "product_quantity": "254 total in the US",
      "reason_for_recall": "Software issue: a violation of 21 CFR 1020.31(a).  After an image is taken, when the user selects and clears an additionally displayed screen the system inhibit is also cleared, allowing the user to take an exposure without the technique factors being displayed.",
      "recall_initiation_date": "20120710",
      "center_classification_date": "20120913",
      "termination_date": "20130110",
      "report_date": "20120919",
      "code_info": "Part Numbers: 5555000-3, 5555000-4, 5555000-5, 5555000-6."
    }
  ]
}