{
  "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": "2026-03-18",
    "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": "90967",
      "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": "Nationwide, Austria, Canada, Egypt, Germany, Hong Kong, Israel, Philippines, Saudi Arabia, South Africa, South Korea, Thailand",
      "recall_number": "Z-0398-2023",
      "product_description": "CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS, 0.7MM TIP OVERALL LENGTH 9-1/2\" (240MM) , REF F-5008",
      "product_quantity": "4 units",
      "reason_for_recall": "XXX",
      "recall_initiation_date": "20221102",
      "center_classification_date": "20221203",
      "report_date": "20221214",
      "code_info": "UDI/DI 10885403041013, ALL LOTS"
    }
  ]
}