{
  "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-0114-2019",
      "product_description": "ADVIA Centaur CKMB Calibrator 2-pack Japan, Cat No. 02562748    Product Usage:  For in vitro diagnostic use in calibrating ADVIA Centaur systems CKMB assays.",
      "product_quantity": "69 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 10333512      Lot # Expiry UDI #  58311A67 2018-Dec-11 (01)00630414056890(10)58311A67(17)20181211  97468A67 2018-Dec-11 (01)00630414056890(10)97468A67(17)20181211"
    }
  ]
}