{
  "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": "Mansfield",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91087",
      "recalling_firm": "Cardinal Health",
      "address_1": "777 West St",
      "address_2": "N/A",
      "postal_code": "02048-1122",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "Z-0356-2023",
      "product_description": "Dover Closed Urethral Tray with Vinyl Catheter 14 Fr/Ch (4.7 ml) 5ml Catheter  Product Code: 2480\t  Intended for urinary drainage from the bladder of a patient",
      "product_quantity": "N/A",
      "reason_for_recall": "Occlusion (blockage) of the bubble inlet port of the urinary drainage bag which may prevent urine draining into the bag. If the bladder is not emptied within a clinically appropriate time, this may increase the risk of urinary retention",
      "recall_initiation_date": "20221101",
      "center_classification_date": "20221202",
      "report_date": "20221214",
      "code_info": "UDI-DI:  Each 10884521009370  Case 20884521009377  Lot Numbers:  2216501464, 2213046064, 2206726764"
    }
  ]
}