{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "140636",
      "product_res_number": "Z-0260-2016",
      "event_date_initiated": "2015-08-31",
      "event_date_posted": "2015-11-10",
      "recall_status": "Terminated",
      "event_date_terminated": "2018-09-07",
      "res_event_number": "72301",
      "product_code": "OUO",
      "k_numbers": [
        "K142098"
      ],
      "product_description": "GE Healthcare, SIGNA PET/MR 3.0T. \n\nProduct Usage:\nThe SIGNA PET/MR system combines magnetic resonance diagnostic devices (MRDD) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high-resolution physiologic and anatomic information, acquired simultaneously and isocentrically.",
      "code_info": "00000000UA0064\t415723SHMRW 00000000UA0217\t415CBMRP N/A\t                    608262PETMR1 \tMAYOPETMR01 \tUABPETMR \tSID TBD \tSID TBD \t262574PETMR1 310974MR1\tMRUA0459 309452MR1\t082427HWBAY1 \tM40345211 N/A\tSID TBD \tSID TBD \tSID TBD 00001309FMM076\tC001MR01 00000309668MR2\tAC001MR02 00000307417MR6\t120810MR03",
      "firm_fei_number": "2126677",
      "recalling_firm": "GE Healthcare",
      "address_1": "3000 N Grandview Blvd",
      "city": "Waukesha",
      "state": "WI",
      "postal_code": "53188-1615",
      "additional_info_contact": "GE Healthcare Service\n800-437-1171",
      "reason_for_recall": "When performing head or neck scans, the currently displayed SAR values could be lower than the actual SAR in the head as predicted by SAR modeling. The predicted HEAD SAR value from the modeling suggests the actual SAR in the head could exceed IEC60601-2-33 limit of 3.2 W/kg for some scans.",
      "root_cause_description": "Software design",
      "action": "GE Healthcare sent an Urgent Medical Device Correction letter dated August 31, 2015.  The letter was addressed to Hospital Administrators/Risk Managers, Radiology Department Managers, & Radiologists.  The letter described the Safety Issue, Safety Instructions, Affected Product Details, Product Correction and Contact Information. For questions contact GE Healthcare Service at 1-800-437-1171 or your local Service Representative.",
      "product_quantity": "17",
      "distribution_pattern": "Worldwide Distribution - US: Nationwide including DC, PR and GU and the countries of ALGERIA, ARGENTINA, AUSTRALIA, AUSTRIA, AZERBAIJAN, BAHRAIN, BELARUS, BELGIUM, BERMUDA, BOSNIA HERZEGOVINA, BRAZIL, BULGARIA, CANADA, CHINA, CZECH REPUBLIC, DENMARK, EGYPT, ESTONIA, ETHIOPIA, FINLAND, FRANCE, GERMANY, GREECE, HONG Kong, HUNGARY, INDIA, INDONESIA, IRAN, IRELAND, ISRAEL, ITALY, JAMAICA, JAPAN, KAZAKHSTAN, REPUBLIC OF KOREA, KUWAIT, LEBANON, LUXEMBOURG, MALAYSIA, MEXICO, NETHERLANDS, NEW ZEALAND, NORWAY, PERU, POLAND, PORTUGAL, QATAR, ROMANIA, RUSSIA, SAUDI ARABIA, SERBIA, SINGAPORE, SLOVENIA, SOUTH AFRICA, SPAIN, SWEDEN, SWITZERLAND, SYRIA, TAIWAN, THAILAND, TURKEY, UNITED ARAB EMIRATES, UNITED KINGDOM, URUGUAY, and VENEZUELA.",
      "openfda": {
        "k_number": [
          "K200213",
          "K183014",
          "K234154",
          "K172531",
          "K192672",
          "K142098",
          "K253963",
          "K103429",
          "K133226",
          "K163234",
          "K253023",
          "K213709",
          "K222540",
          "K103483",
          "K163619"
        ],
        "registration_number": [
          "2247992",
          "3015329423",
          "3011015597",
          "3011950073",
          "3002808157",
          "3015232217",
          "1529041",
          "3004754211",
          "3005326970",
          "2183553",
          "3010949642"
        ],
        "fei_number": [
          "3015329423",
          "3011015597",
          "3011950073",
          "3002808157",
          "3015232217",
          "1000208827",
          "3004754211",
          "3005326970",
          "3005214683",
          "2183553",
          "3010949642"
        ],
        "device_name": "Tomographic Imager Combining Emission Computed Tomography With Nuclear Magnetic Resonance",
        "medical_specialty_description": "Radiology",
        "regulation_number": "892.1200",
        "device_class": "2"
      }
    }
  ]
}