{
  "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-0361-2023",
      "product_description": "Dover Closed Urethral Tray with Vinyl Catheter 14 Fr/Ch (4.7 mm), 5 mL Catheter Pre-connected to 1000 mL Drainage Bag  Product Code: 3450LF    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 10884521009585  Case  20884521009582  Lot Numbers:   2216806064, 2214452064, 2212401164 2210219764, 2209525364, 2208816464 2206737964, 2206727564"
    }
  ]
}