{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Tarrytown",
      "address_1": "511 Benedict Ave",
      "reason_for_recall": "Valves used on the Atellica CH 930, Atellica IM 1300 and Atellica IM 1600 analyzers may develop a malfunction due to a manufacturing defect and may result in the valve wearing and leaking over time. The leaking is a risk in valves subject to high pressure or high wear and may impact the result accuracy of any assay.",
      "address_2": "",
      "product_quantity": "US: 210\tOUS: 874",
      "code_info": "Effected SN Range:  CM00902 - CM02065    Note: xxxx in serial number is any number.     UDI:  00630414002163",
      "center_classification_date": "20210707",
      "distribution_pattern": "Nationwide  Foreign:  Country Name  Algeria  Argentina  Australia  Austria  Bahrain  Bangladesh  Belgium  Brazil  Bulgaria  Burkina Faso  Canada  Chile  Colombia  Croatia  Cura¿ao  Cyprus  Czech Republic  Denmark  Ecuador  Egypt  Estonia  Finland  France  Germany  Greece  Hungary  India  Indonesia  Iraq  Ireland  Israel  Italy  Japan  Kenya  Kuwait  Latvia  Libya  Lithuania  Malaysia  Mexico  Morocco  Netherlands  New Zealand  Norway  Oman  P.R. China  Pakistan  Peru  Philippines  Poland  Portugal  Qatar  Republic Korea  Romania  Russian Fed.  Saudi Arabia  Singapore  Slovakia  Slovenia  South Africa  Spain  Sweden  Switzerland  Taiwan  Thailand  Turkey  U.A.E.  Uganda  Ukraine  United Kingdom  Uruguay  Vatikancity  Vietnam",
      "state": "NY",
      "product_description": "Atellica CH 930 Analyzer -  multi-component system for in vitro diagnostic testing of clinical specimens  SMN 11067000",
      "report_date": "20210714",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Healthcare Diagnostics, Inc.",
      "recall_number": "Z-2026-2021",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "88056",
      "more_code_info": "",
      "recall_initiation_date": "20210513",
      "postal_code": "10591-5005",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}