{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Molndal",
      "state": "N/A",
      "country": "Sweden",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85905",
      "recalling_firm": "Wellspect HealthCare (Division of DENTSPLY IH AB)",
      "address_1": "Aminogatan 1",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "AL, AZ, CA, CT, FL, GA, IL, IN, KY, MA, MD, MI, MO, NC, NH, NJ, OH, PA, RI, SC, TX, VA and Australia, Brazil, Canada, European Union, China, South Korea, Kuwait, New Zeeland, Singapore, United Kingdom",
      "recall_number": "Z-2643-2020",
      "product_description": "LoFric Origo, Nelaton, 16in, FR10 urinary catheters",
      "product_quantity": "N/A",
      "reason_for_recall": "Wellspect Healthcare is voluntarily recalling certain LoFric¿ Origo\" urethral catheters due to a potential defect which may be present in the catheter s distal tip.",
      "recall_initiation_date": "20200617",
      "center_classification_date": "20200717",
      "termination_date": "20210409",
      "report_date": "20200729",
      "code_info": "Lot # 447123",
      "more_code_info": ""
    }
  ]
}