{
  "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-1513-2013",
      "product_description": "ADVIA Centaur¿ iPTH ReadyPack Assay 500 Tests; REF 10492369, 10493615, 1049361.    For in vitro diagnostic use in the quantitative determination of intact parathyroid hormone (iPTH).",
      "product_quantity": "3302  Kits (500 test)",
      "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": "Reagent Lot Numbers: 056301 and 56302  Kit Lot Number/Exp. Date:  REF 10492369- 500 Tests  61639301 09 Nov 2011  REF 1 0493615 - 500 Tests  63607301 09 Nov 2011  68004301 09 Nov 2011  70229301 09 Nov 2011  74126301 09Nov2011  REF 10493616-500 Tests  62645302 09 Nov 2011  66612302 09 Nov 2011  74129302 09 Nov 2011"
    }
  ]
}