{
  "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": "2026-04-15",
    "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": "72943",
      "recalling_firm": "GE Medical Systems, 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 including PR except NH,  VT, & WY.  Internationally to ALBANIA, ALGERIA, ARGENTINA, AUSTRALIA, AUSTRIA, BANGLADESH, BELGIUM, BOLIVIA, BOSNIA, BRAZIL, CAMBODIA, CANADA, CHILE, CHINA, COLOMBIA, COSTA RICA, CZECH REPUBLIC, DENMARK, ECUADOR, EGYPT, ESTONIA, FINLAND, FRANCE, GEORGIA, GERMANY, CHANA, GIBRALTAR, GREECE, GUATEMALA, HONG KONG, HUNGARY, ICELAND, INDIA, INDONESIA, IRAQ, IRELAND, ISRAEL, ITALY, JAPAN, JORDAN, KAZAKHSTAN KENYA, REPUBLIC OF KOREA, KUWAIT, LATVIA, LITHUANIA,MALAYSIA, MALDIVES, MARTINIQUE, MEXICO, MOROCCO, NETHERLANDS, NEW ZEALAND, NICARAGUA, NORWAY, OMAN, PAKISTAN, PERU, PHILIPPINES, POLAND, QATAR, REUNION, ROMANIA, RUSSIAN FEDERATION SAUDI ARABIA, SERBIA, SINGAPORE, SLOVAKIA, SOUTH AFRICA, SPAIN, SRI lanka, SWEDEN, SWITZERLAND, TAIWAN, THAILAND, TURKEY, UNITED ARAB EMIRATES, UNITED KINGDOM, VENEZUELA, VIETNAM.",
      "recall_number": "Z-0679-2016",
      "product_description": "GE Healthcare, Aestiva MRI, 1006-9310-000.  This version of the Datex-Ohmeda 7900 ventilator is used in Datex-Ohmeda Aestiva/5 anesthesia systems. It is a microprocessor based, electronically controlled, pneumatically driven ventilator that provides patient ventilation during surgical procedures. The Aestiva/5 MRI anesthesia system provides the functional feature set offered by the conventional Aestiva/5 to the clinician with the added ability to be used in the MR environment.",
      "product_quantity": "84",
      "reason_for_recall": "The Drive Gas Check Valve of certain Anesthesia products could become stuck in a fixed open position, which could cause pressure to build in the mechanical ventilation cycle. If this issue is left unresolved, it could result in excessive or prolonged pressure in the patient breathing circuit during ventilation potentially resulting in barotrauma.",
      "recall_initiation_date": "20151215",
      "center_classification_date": "20160121",
      "termination_date": "20160921",
      "report_date": "20160127",
      "code_info": "AMTU01048  AMTU01023  AMTU00163  AMTU01050  AMTU00172  AMTU00175  AMTU00176  AMTU01034  AMTU01047  AMTU01055  AMTU01001  AMTU01002  AMTU01021  AMTU01044  AMTU01042  AMTU01015  AMTU00178  AMTU00179  AMTU00162  AMTU01000  AMTU01012  AMTU01041  AMTU00167  AMTU01019  AMTU00177  AMTU01049  AMTU00171  AMTU00164  AMTU01066  AMTU01006  AMTU00168  AMTU01061  AMTU01060  AMTU01056  AMTU01057  AMTU01073  AMTU00154  AMTU00166  AMTU00174  AMTU01005  AMTU01035  AMTU00150  AMTU01024  AMTU01025  AMTU01026  AMTU01027  AMTU01037  AMTU00152  AMTU01040  AMTU01022  AMTU00157  AMTU00158  AMTU00159  AMTU00160  AMTU00170  AMTU01018  AMTU01009  AMTU01032  AMTU01046  AMTU01045  AMTU01020  AMTU01008  AMTU00165  AMTU01013  AMTU01014  AMTU01033  AMTU01016  AMTU01036  AMTU01038  AMTU00151  AMTU00169  AMTU01003  AMTU00161  AMTU01010  AMTU01064  AMTU01011  AMTU01004  AMTU01017  AMTU01031  AMTU01053  AMTU01058  AMTU01059  AMTU01039  AMTU01007",
      "more_code_info": ""
    }
  ]
}