{
  "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": "Tarrytown",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "67603",
      "recalling_firm": "Siemens Healthcare Diagnostics",
      "address_1": "511 Benedict Ave",
      "address_2": "N/A",
      "postal_code": "10591-5005",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide and internationally",
      "recall_number": "Z-1553-2014",
      "product_description": "ADVIA Centaur XP Immunoassay system, an automated in vitro diagnostic analyzer. Catalog # 078-A011-03 - ADVIA Centaur XP, Catalog # 078-A011R03 - ADVIA Centaur XP refurb.",
      "product_quantity": "5,900 units total (1,679 domestically & 4,221 internationally)",
      "reason_for_recall": "Instrument Cover Gas Spring failures.  Over time, the gas spring may lose its effectiveness and fail to support the cover in its full or partially open position.  This may lead to the cover falling.",
      "recall_initiation_date": "20140218",
      "center_classification_date": "20140506",
      "termination_date": "20170306",
      "report_date": "20140514",
      "code_info": "All serial numbers of Catalog # 078-A011-03 - ADVIA Centaur XP and Catalog # 078-A011R03 - ADVIA Centaur XP refurb."
    }
  ]
}