{
  "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": "2026-05-06",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Waukesha",
      "address_1": "3000 N Grandview Blvd",
      "reason_for_recall": "An incident was reported that an operator's finger was pinched between the fixed roller and the gliding tabletop of a Proteus XR/a Table while moving the tabletop with the thumb placed over its edge and fingers underneath",
      "address_2": "",
      "product_quantity": "3,796 units",
      "code_info": "All serial numbers",
      "center_classification_date": "20120608",
      "distribution_pattern": "Worldwide Distribution.",
      "state": "WI",
      "product_description": "GE  Proteus XR/a Radiographic System. GE Medical Systems-Americas Milwaukee, WI.  Model Number: 2259988.    Product is indicated for use in generating radiographic images of human anatomy in all general-purpose diagnostic procedures. This device is not intended for mammographic applications.",
      "report_date": "20120620",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "General Electric Med Systems LLC",
      "recall_number": "Z-1790-2012",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "37654",
      "termination_date": "20120731",
      "more_code_info": "",
      "recall_initiation_date": "20060531",
      "postal_code": "53188-1615",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}