{
  "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": [
    {
      "status": "Terminated",
      "city": "East Walpole",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80954",
      "recalling_firm": "Siemens Healthcare Diagnostics, Inc",
      "address_1": "333 Coney St",
      "address_2": "N/A",
      "postal_code": "02032-1516",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-0113-2019",
      "product_description": "ADVIA Centaur CKMB Calibrator, Cat No. 09318028    Product Usage:  For in vitro diagnostic use in calibrating ADVIA Centaur systems CKMB assays.",
      "product_quantity": "1870 kits",
      "reason_for_recall": "A potential bias was identified with certain kits compared to the internal standards.",
      "recall_initiation_date": "20180724",
      "center_classification_date": "20181015",
      "termination_date": "20200526",
      "report_date": "20181024",
      "code_info": "SMN 10311570    Lot # Expiry UDI #  57834A64 2018-Dec-11 (01)00630414124803(10)57834A64(17)20181211  57835A64 2018-Dec-11 (01)00630414124803(10)57835A64(17)20181211  72519A64 2018-Dec-11 (01)00630414124803(10)72519A64(17)20181211  98115A64 2018-Dec-11 (01)00630414124803(10)98115A64(17)20181211"
    }
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}