{
  "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": "East Walpole",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "64610",
      "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": "Nationwide Distribution.",
      "recall_number": "Z-1119-2013",
      "product_description": "ADVIA Centaur Vitamin D Assay (100 tests); Reference Number: 10491994.    For use in the quantitative determination of Vit D.",
      "product_quantity": "3871",
      "reason_for_recall": "Negative bias in patient samples for Vitamin D",
      "recall_initiation_date": "20130313",
      "center_classification_date": "20130415",
      "termination_date": "20150305",
      "report_date": "20130424",
      "code_info": "Ready Pack Lot Number:  134009  Kit Lot  Number/Exp. Date:  88766009 4/28/2013  88786009 4/28/2013  89198009 4/28/2013  Ready Pack Lot Number:  134010  Kit Lot  Number/Exp. Date:  90671010 6/2/2013  92212010 6/2/2013    Ready Pack Lot Number:  134011  Kit Lot  Number/Exp. Date:   92395011 8/12/2013  94660011 8/12/2013  95016011 8/12/2013  95313011 8/12/2013"
    }
  ]
}