{
  "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": "2026-09-10",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 4
    }
  },
  "results": [
    {
      "cfres_id": "217687",
      "product_res_number": "Z-1044-2026",
      "event_date_initiated": "2025-12-10",
      "event_date_posted": "2026-01-09",
      "recall_status": "Open, Classified",
      "res_event_number": "98133",
      "product_code": "IYX",
      "k_numbers": [
        "K894931"
      ],
      "product_description": "SMV DSX New Line, \n\nSystem, Tomography, Computed, Emission",
      "code_info": "UDI/DI Not applicable:  All serial numbers in distribution",
      "firm_fei_number": "3004571294",
      "recalling_firm": "GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING",
      "address_1": "4, Hayozma St 4 Hayozma St",
      "city": "Tirat Carmel",
      "country": "Israel",
      "reason_for_recall": "GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service (herein referred to as  Impacted Systems  and\nlisted in the Affected Product Details section of this letter) could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.  \nThere have been no reports of detector falls or injuries as a result of this potential issue.  \nThe Impacted Systems affected by this notice are those that have not been manufactured for several years. GE HealthCare has previously communicated End of Guaranteed Service for these Impacted Systems.",
      "root_cause_description": "Package design/selection",
      "action": "GE Healthcare began notifying their consignees by telephone on 12/10/2025, followed by an URGENT MEDICAL DEVICE CORRECTION UPDATE notice distributed on 01/05/2025 via US mail.  The notice explained the issue, safety risk, and requested the consignee stop use of the product.  Care should be exercised when deinstalling these systems.  To discuss replacement options, your GE HealthCare account representative. Should be contacted.",
      "product_quantity": "7 units",
      "distribution_pattern": "US, Brazil, Egypt, Canada, Mexico, Turkey, Italy, Sweden, Switzerland, France, Spain Chile, Germany, Iran, Greece",
      "openfda": {
        "k_number": [
          "K850463",
          "K771599",
          "K813073",
          "K852089",
          "K875198",
          "K904050",
          "K780971",
          "K853470",
          "K790081",
          "K833821",
          "K780855",
          "K881013",
          "K770343",
          "K885054",
          "K882312",
          "K143156",
          "K934766",
          "K040587",
          "K033960",
          "K926550",
          "K852648",
          "K071195",
          "K230221",
          "K780491",
          "K781739",
          "K811676",
          "K162052",
          "K081829",
          "K110384",
          "K160933",
          "K843288",
          "K911346",
          "K904174",
          "K110601",
          "K801654",
          "K840052",
          "K820244",
          "K924639",
          "K062141",
          "K761159",
          "K020643",
          "K843716",
          "K905412",
          "K770753",
          "K123408",
          "K893379",
          "K212587",
          "K984466",
          "K872297",
          "K093706",
          "K101391",
          "K802475",
          "K092471",
          "K885242",
          "K923356",
          "K932673",
          "K780165",
          "K850397",
          "K930283",
          "K841906",
          "K943602",
          "K811629",
          "K102231",
          "K853482",
          "K923180",
          "K871175",
          "K884675",
          "K884661",
          "K884674",
          "K945792",
          "K023373",
          "K801653",
          "K880878",
          "K924878",
          "K100838",
          "K770531",
          "K790499",
          "K910967",
          "K894931",
          "K003775",
          "K791682",
          "K790463",
          "K832505",
          "K844218",
          "K870703",
          "K843558",
          "K903988",
          "K884672",
          "K933256",
          "K163687",
          "K870818",
          "K073456",
          "K932957",
          "K900689",
          "K905074",
          "K111791",
          "K833811",
          "K903030",
          "K810974",
          "K811715",
          "K900773",
          "K780060",
          "K052473",
          "K782047",
          "K935273",
          "K051402",
          "K903469",
          "K872127",
          "K801368",
          "K082588",
          "K790466",
          "K770954",
          "K993813",
          "K932701",
          "K022342",
          "K851644",
          "K781673",
          "K921296",
          "K780969",
          "K081757",
          "K841964",
          "K782029",
          "K811187",
          "K926083",
          "K780155",
          "K861637",
          "K884673",
          "K905827",
          "K961104",
          "K933513"
        ],
        "registration_number": [
          "3017754782",
          "2031050",
          "2433682",
          "3005496266",
          "3008962177",
          "2020678",
          "3002807315",
          "3009470597",
          "3030186509",
          "3014954414",
          "3005128583",
          "3027338963",
          "9710645",
          "3023006704",
          "3004363352",
          "9613299",
          "2132111",
          "1423348",
          "3006611212",
          "3015232217",
          "3005945241"
        ],
        "fei_number": [
          "3017754782",
          "2433682",
          "3005496266",
          "1000140026",
          "3008962177",
          "3001236767",
          "2020678",
          "3002807315",
          "3009470597",
          "3000210013",
          "3030186509",
          "3014954414",
          "3005128583",
          "3027338963",
          "3002831423",
          "3023006704",
          "3004363352",
          "3006611212",
          "3015232217",
          "3005945241",
          "3004571294"
        ],
        "device_name": "Camera, Scintillation (Gamma)",
        "medical_specialty_description": "Radiology",
        "regulation_number": "892.1100",
        "device_class": "1"
      }
    }
  ]
}