{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Waltham",
      "state": "MA",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "75949",
      "recalling_firm": "PerkinElmer Health Sciences, Inc.",
      "address_1": "940 Winter St",
      "address_2": "N/A",
      "postal_code": "02451-1457",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US Nationwide in the state of MN and countries of  China, India, Philippines, France, South Korea, Vietnam, Taiwan, Morocco, Kazachstan, UK, Spain, and  Israel,",
      "recall_number": "Z-1101-2017",
      "product_description": "Program Update Package AutoDELFIA¿ 3.0, Fluorometer, for clinical use  Product Number: 1235-8110    Product Usage:  The Wallac 1235 AutoDELFIA automatic immunoassay system is designed to automatically perform assays using the DELFIA technology. DELFIA technology is based on the proven and widely used method of time resolved fluorometry",
      "product_quantity": "1 unit (US) 2 units (OUS)",
      "reason_for_recall": "AutoDELFIA System with Version 3.0 Software: Potential plate loading failures",
      "recall_initiation_date": "20161221",
      "center_classification_date": "20170126",
      "termination_date": "20181003",
      "report_date": "20170201",
      "code_info": "Batch Code: 649552    OUS: 649552, 649552"
    }
  ]
}