{
  "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": [
    {
      "country": "United States",
      "city": "Irvine",
      "address_1": "33 Technology Dr",
      "reason_for_recall": "Advanced Sterilization Products (ASP) is recalling the STERRAD NX, STERRAD 50, and STERRAD 100S Sterilization Systems because some healthcare workers detected odors or smells possibly emanating from STERRAD Systems.",
      "address_2": "",
      "product_quantity": "5584 units",
      "code_info": "not available",
      "center_classification_date": "20140114",
      "distribution_pattern": "Nationwide Distribution",
      "state": "CA",
      "product_description": "STERRAD NX Sterilization System, Product Code: 10033    The STERRAD NX Sterilization System is a general purpose, low temperature sterilizer which uses the STERRAD NX process to inactivate microorganisms on a broad range of medical devices and surgical instruments.",
      "report_date": "20140122",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Advanced Sterilization Products",
      "recall_number": "Z-0744-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "67043",
      "termination_date": "20140327",
      "more_code_info": "",
      "recall_initiation_date": "20131216",
      "postal_code": "92618-2346",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}