{
  "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,
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    }
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  "results": [
    {
      "status": "Terminated",
      "city": "Washington",
      "state": "",
      "country": "United Kingdom",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83587",
      "recalling_firm": "Rocket Medical Plc",
      "address_1": "Industrial Estate Sedling Road Wear Indu",
      "address_2": "Tyne & Wear",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "Z-0512-2020",
      "product_description": "Rocket KCH Fetal Bladder Drainage Catheter  Model: R57405",
      "product_quantity": "1081",
      "reason_for_recall": "A complaint was received regarding kinking of the device prior to use. If a device is kinked it cannot be used. In addition, the company became aware that the device had been used for pleural drainage, which is not included in the device indications.",
      "recall_initiation_date": "20190801",
      "center_classification_date": "20191126",
      "termination_date": "20211102",
      "report_date": "20191204",
      "code_info": "All lots  (UDI): 05055270913678",
      "more_code_info": ""
    }
  ]
}