{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Vernon Hills",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90958",
      "recalling_firm": "Carefusion 2200 Inc",
      "address_1": "75 N Fairway Dr",
      "address_2": "N/A",
      "postal_code": "60061-1845",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US and Australia, Bahrain, Canada, Denmark, Hong Kong, Italy, Japan, Malaysia, Mexico, Norway, Philippines, Saudi Arabia, Singapore, South Africa, Sweden, Thailand, UK, United Arab Emirates",
      "recall_number": "Z-0212-2023",
      "product_description": "CareFusion V.Mueller GENESIS FULL-LENGTH CONTAINER 23 X12\" (58.4 X 30.5CM) 4\" (10CM) DEEP STERRAD COMPATIBLE, REF CD3-4ST",
      "product_quantity": "308 units",
      "reason_for_recall": "Genesis STERRAD Reusable Rigid Sterilization Containers have not consistently met the requirements for aerosol challenge testing.",
      "recall_initiation_date": "20220926",
      "center_classification_date": "20221111",
      "report_date": "20221123",
      "code_info": "UDI/DI (01) 10885403019319, ALL LOTS"
    }
  ]
}