{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Mansfield",
      "address_1": "15 Hampshire St",
      "reason_for_recall": "Medtronic is voluntarily recalling one lot of its  MAHURKAR\"* Elite 12 FR x 16cm Acute Dual Lumen Dialysis Catheter with Curved Extensions, IC Trays, Lot 1717900160, following notification from our supplier that one production lot of MAHURKAR\"* Elite 12 FR x 16cm Acute Dual Lumen Dialysis Catheter with Curved Extensions, IC Trays was inadvertently shipped to Medtronic and distributed without being sterilized.",
      "address_2": "",
      "product_quantity": "",
      "code_info": "UDI: 10884521126473/20884521126470  Lot: 1717900160.",
      "center_classification_date": "20180314",
      "distribution_pattern": "U.S.",
      "state": "MA",
      "product_description": "MAHURKAR\"* Elite 12 FR x 16cm Acute Dual Lumen Dialysis  Catheter with Curved Extensions, IC Trays. Product Number: 8888222316.",
      "report_date": "20180321",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Medtronic Minimally Invasive Therapies Group",
      "recall_number": "Z-1007-2018",
      "initial_firm_notification": "Telephone",
      "product_type": "Devices",
      "event_id": "79319",
      "termination_date": "20180615",
      "more_code_info": "",
      "recall_initiation_date": "20171014",
      "postal_code": "02048-1113",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}