{
  "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": "65224",
      "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-1514-2013",
      "product_description": "ADVIA Centaur iPTH Calibrator 2 pk; REF 10492394.    For in vitro diagnostic use in calibrating Intact PTH assays.",
      "product_quantity": "99 (2 pk)",
      "reason_for_recall": "iPTH Assay- reagent and calibrator lots may have demonstrated higher than anticipated variability",
      "recall_initiation_date": "20130514",
      "center_classification_date": "20130606",
      "termination_date": "20150305",
      "report_date": "20130612",
      "code_info": "Calibrator Lot Number: C5601 and C5602  Kit Lot Number/Exp. Date:  61405A01 27 Oct 2011  66517A02 27 Oct 2011  66611A02 27 Oct 2011  71997C02 27 Oct 2011"
    }
  ]
}