{
  "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": "233 units",
      "code_info": "not available",
      "center_classification_date": "20140114",
      "distribution_pattern": "Nationwide Distribution",
      "state": "CA",
      "product_description": "STERRAD 50 Sterilization System, Product Code: 10050  The STERRAD 50 Sterilization System is a general purpose, low temperature sterilizer which uses the STERRAD 50 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-0745-2014",
      "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"
    }
  ]
}