{
  "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": "Irvine",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71708",
      "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-2459-2015",
      "product_description": "CIDEX Activated Dialdehyde Solution, 4 bottles/case, P/N: 2266",
      "product_quantity": "23,426 cases",
      "reason_for_recall": "Advanced Sterilization Products (ASP) is recalling the CIDEX Activated Dialdehyde Solution because it may lack the adequate data to support the entire 24-month shelf life.",
      "recall_initiation_date": "20150727",
      "center_classification_date": "20150825",
      "termination_date": "20160706",
      "report_date": "20150902",
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