{
  "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": [
    {
      "country": "United States",
      "city": "Newark",
      "address_1": "500 Gbc Dr Ms 514",
      "reason_for_recall": "In March, Siemens Healthcare Diagnostics issued an Urgent Medical Device Correction for decreased recovery of patient samples with the Dimension Vista® CSA & CSAE Flex® reagent cartridges when whole blood samples are run from Small Sample Containers (SSC). Siemens has confirmed that when whole blood samples are run from SSC, HbA1c values may exhibit a percent bias ranging from - 8.2% t",
      "address_2": "PO BOX 6101",
      "product_quantity": "20043",
      "code_info": "catalog #K3105A, material #10470481, All in-date lots",
      "center_classification_date": "20141024",
      "distribution_pattern": "Worldwide Distribution: US (nationwide) and country of: Canada.",
      "state": "DE",
      "product_description": "Dimension Vista¿ HbA1c",
      "report_date": "20141105",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Healthcare Diagnostics, Inc.",
      "recall_number": "Z-0127-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "69334",
      "termination_date": "20150810",
      "more_code_info": "",
      "recall_initiation_date": "20140814",
      "postal_code": "19702-2466",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}