{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Tyne & Wear",
      "state": "",
      "country": "United Kingdom",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97994",
      "recalling_firm": "Rocket Medical Plc",
      "address_1": "Industrial Estate Sedling Road Wear Industrial Estate",
      "address_2": "Washington",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Domestic: CO, CT, IL, MA, ME, NH, NJ, NM, OH, RI, SC, TX;  International: UAE, Austria, Australia, Canada, Germany, Denmark, Finland, France, United Kingdom, Greece, Hong Kong, Ireland, Israel, India, Italy, Jersey, Kenya, Sri Lanka, Malta, Netherlands, Norway, New Zealand, Portugal, Saudi Arabia, Singapore, Slovenia, South Africa",
      "recall_number": "Z-0952-2026",
      "product_description": "Brand Name: Rocket  Product Name: Rocket 18Fg Seldinger Catheter Procedure Tray  Model/Catalog Number: R54544-18-PK  Software Version: N/A  Product Description: Chest tube manufactured from PVC, with fenestrations and a barium stripe to the indicated French gauge size. Supplied with a procedure pack to allow percutaneous insertion, supplied with connectors to allow attachment to chest drain bottle devices.  Component: N/A",
      "product_quantity": "630 units",
      "reason_for_recall": "IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.",
      "recall_initiation_date": "20251107",
      "center_classification_date": "20251218",
      "report_date": "20251224",
      "code_info": "Model/Catalog Number: R54544-18-PK; UDI-DI: 050552709TF06DXY; Lot Code: 496899, 500956, 497076, 501169, 497584, 501188, 499227, 502430, 499417, 502951, 499461, 503306, 499897, 503430, 499898, 503529, 499899, 504180, 499908, 504543, 500407, 504823, 500477;",
      "more_code_info": ""
    }
  ]
}