{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "51198",
      "product_res_number": "Z-0720-2007",
      "event_date_initiated": "2007-03-16",
      "event_date_posted": "2007-04-05",
      "recall_status": "Terminated",
      "event_date_terminated": "2007-05-25",
      "res_event_number": "37638",
      "product_code": "MEQ",
      "pma_numbers": [
        "P970008"
      ],
      "product_description": "Urologix Microwave Delivery System 3.0 - 5.0.  For use with prostatic urethra lengths of 3.0-5.0 cm only.  Model TA1121D.",
      "code_info": "Individual Catheter lot numbers:  M002671,M002672, M002589 and M002736 for model TA1121D.    Kit box lot numbers:  KP011206, KP053006B, KP053006C, KP060205, KP0011206.",
      "firm_fei_number": "3000718675",
      "recalling_firm": "Urologix, Inc.",
      "address_1": "14405 21st Ave N",
      "city": "Minneapolis",
      "state": "MN",
      "postal_code": "55447-4685",
      "reason_for_recall": "The catheter in the kit matches the description on the kit and pouch label; however, an incorrect label was placed onto the catheter during manufacturing.",
      "root_cause_description": "Other",
      "action": "A letter dated 3/16/07 was FedEx overnight to consignees.  The letter described the product, problem and gave instructions for returning and replacing the affected product.",
      "product_quantity": "96",
      "distribution_pattern": "Nationwide and the Netherlands.",
      "openfda": {
        "pma_number": [
          "P970008",
          "P030006",
          "P950014",
          "P010055",
          "P970044",
          "P000043"
        ],
        "registration_number": [
          "1721676",
          "3009969279",
          "2183744",
          "2183967",
          "3007029079",
          "2133936",
          "2025851",
          "3010806653"
        ],
        "fei_number": [
          "1721676",
          "3009969279",
          "2183744",
          "3000718675",
          "3007029079",
          "1000115735",
          "2025851",
          "3010806653"
        ],
        "device_name": "System, Hyperthermia, Rf/Microwave (Benign Prostatic Hyperplasia),Thermotherapy",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3"
      }
    }
  ]
}