{
  "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": "Morrisville",
      "state": "NC",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81954",
      "recalling_firm": "Teleflex Medical",
      "address_1": "3015 Carrington Mill Blvd",
      "address_2": "N/A",
      "postal_code": "27560-5437",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution: US (nationwide) and countries of: Canada, Bolivia, Guatemala, Jamaica, Peru, Trinidad, and El Salvador.",
      "recall_number": "Z-1975-2019",
      "product_description": "RUSCH Urinary Drainage bag, 2000mlm REF 390060     urine collection device",
      "product_quantity": "76725 US eaches",
      "reason_for_recall": "The device labels are not UDI compliant. The missing UDI compliance information on the labelling would not affect the function/performance of the device itself. Other label information and warnings are unaffected by this labelling.",
      "recall_initiation_date": "20190114",
      "center_classification_date": "20190715",
      "termination_date": "20221213",
      "report_date": "20190724",
      "code_info": "GTIN: 14026704645715    Lot/Batch Numbers:  20161005  20161120  20161125  20170105  20170210  20170401  20170402  20170501   20170801  20170901  20170902   20170903  20170904  20171101  20170701"
    }
  ]
}