{
  "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": "Irvine",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "64692",
      "recalling_firm": "Advanced Sterilization Products",
      "address_1": "33 Technology Dr",
      "address_2": "N/A",
      "postal_code": "92618-2346",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-1027-2013",
      "product_description": "STERRAD 200 Sterilization System, P/N 10201    Product Usage:  The STERRAD 200 Sterilization System is a general purpose, low temperature sterilizer which uses the STERRAD 200 process to inactivate microorganisms on a board range of medical devices and surgical instruments.",
      "product_quantity": "1038 units",
      "reason_for_recall": "The recall was initiated because Advanced Sterilization Products (ASP) has determined that the STERRAD 100NX and STERRAD 200 Sterilization Systems may emit an odor or smell into the surrounding environment that is not typical to normal operating conditions.",
      "recall_initiation_date": "20130322",
      "center_classification_date": "20130329",
      "termination_date": "20130930",
      "report_date": "20130410",
      "code_info": "Codes:    10217  10201-002  10201  10202-001"
    }
  ]
}