{
  "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": "65958",
      "recalling_firm": "GE Healthcare, LLC",
      "address_1": "3000 N Grandview Blvd",
      "address_2": "",
      "postal_code": "53188-1615",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution-USA (nationwide) including the states of AZ, CA, CO, FL, GA, IL, IA, IS, LA, MA, MO, NH, NM, NY, OH, OK PA, SC, TX, UT, VA, WA, and WI, and the countries of UNITED KINGDOM, DENMARK, CHILE, ALGERIA, ARGENTINA, AUSTRALIA, AUSTRIA, AZERBAIJAN, BAHRAIN, BELGIUM, CANADA, CZECH REPUBLIC, ECUADOR, EGYPT, ETHIOPIA, FINLAND, FRANCE, FRANCE GUIANA, GERMANY, GUADELOUPE, GUATEMALA, GUYANA, INDIA, INDONESIA, IRAQ, ITALY, JAPAN, JORDAN, KAZAHSTAN, KOREA, KUWAIT, LATVIA, MYANMA, NETHERLANDS, NEW ZEALAND, NORWAY, PAKISTAN, POLAND, ROMANIA, RUSSIA, SAUDI ARABIA, SOUTH AFRICA, SPAIN, SWEDEN SWITZERLAND, TAIWAN, THAILAND, TURKEY, UKRAINE, UZBEKISTAN, and VIETNAM.",
      "recall_number": "Z-0024-2014",
      "product_description": "GE PET Discovery 610, PET Discovery 710.    Intended for head and whole body attenuation corrected Positron Emission Tomography (PET) imaging.",
      "product_quantity": "28 (4 US & 24OUS)",
      "reason_for_recall": "GE Healthcare has recently become aware of a potential safety issue related with the DMPR function and Screen Saved Images on your scanner which involves Optima CT660, Brivo CT385, Discovery PET/CT 610, Discovery PET/CT 710. The DMPR and Screen Save functionality may possibly generate the same  Series UID. It has been seen that some PACS may combine series under a patient using only the Series UID",
      "recall_initiation_date": "20130326",
      "center_classification_date": "20131017",
      "termination_date": "20131205",
      "report_date": "20131023",
      "code_info": "MfgLotorSerial#  00000428413CN9  00000429077CN1  00000429247CN0  00000430152CN9  00000430656CN9  00000430999CN3  00000431369CN8  00000429701CN6  00000430064CN6  00000431187CN4  00000429354CN4  00000431447CN2  00000293950HM2  00000429821CN2  00000429946CN7  00000430001CN8  00000293950HM2  00000430632CN0  Shipped  Shipped  Shipped  00000429572CN1  00000428755CN3  00000428755CN3  00000428868CN4  00000293949HM4  00000428536CN7  00000429820CN4",
      "more_code_info": ""
    }
  ]
}