{
  "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": "Denzlingen",
      "state": "N/A",
      "country": "Germany",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92700",
      "recalling_firm": "Scholly Fiberoptic Gmbh",
      "address_1": "Robert-Bosch-Str. 1-3",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Nationwide Foreign: Japan, South Korea",
      "recall_number": "Z-2364-2023",
      "product_description": "UroLift Visual Obturator, 20Ch-The visual obturator is used with the UroLift¿ system. Instrument for insertion of a cystoscope shaft into the bladder.  Model: UL-VO",
      "product_quantity": "98 units",
      "reason_for_recall": "There is an improperly performed weld between the cone of the sheath lock and tube of the obturator; mechanical load capacity is impaired, and fracture of the welded joint may occur. Contamination can  occur in this capillary gap, which is not covered by the reprocessing validations performed.",
      "recall_initiation_date": "20230623",
      "center_classification_date": "20230809",
      "report_date": "20230816",
      "code_info": "UDI-DI: 04250480106617 Lot Number: 141980"
    }
  ]
}