{
  "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",
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      "cfres_id": "161506",
      "product_res_number": "Z-0720-2018",
      "event_date_initiated": "2017-07-28",
      "event_date_created": "2018-02-26",
      "recall_status": "Terminated",
      "event_date_terminated": "2019-04-03",
      "res_event_number": "79170",
      "product_code": "CDP",
      "k_numbers": [
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      "product_description": "ADVIA Centaur T3\n\nADVIA Centaur T3: For in vitro diagnostic use in the quantitative determination of triiodothyronine (T3) in serum using the ADVIA Centaur, ADVIA Centaur XP, and ADVIA Centaur XPT systems. Measurements of triiodothyronine are used in the diagnosis and treatment of thyroid disease.",
      "code_info": "x",
      "firm_fei_number": "1219913",
      "recalling_firm": "Siemens Healthcare Diagnostics, Inc",
      "address_1": "333 Coney St",
      "city": "East Walpole",
      "state": "MA",
      "postal_code": "02032-1516",
      "additional_info_contact": "508-668-5000",
      "reason_for_recall": "Siemens has identified an issue when scanning the 20 barcode for the Master Curve Card\n(MCC) with ADVIA Centaur systems T3 kit lots ending in 198 on the ADVIA Centaur XPT\nsystem.",
      "root_cause_description": "Under Investigation by firm",
      "action": "Siemens sent an Urgent Medical Device Correction letter dated July 28, 2017,  that was distributed to all customers in the United States and an Urgent Field Safety Notice was distributed to all customers outside the United States. On August 15, 2017 Follow-up communication was sent to all customers.\n\nFor further questions, please call (508) 668-5000.",
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