{
  "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": "Bloomington",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82026",
      "recalling_firm": "Cook Inc.",
      "address_1": "750 N Daniels Way",
      "address_2": "N/A",
      "postal_code": "47404-9120",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Domestic distribution to nationwide US.    Foreign distribution to Australia, Belgium,  Bolivia, Canada, Canary Islands, Chile, China, Colombia, Croatia, Czech Republic,  Denmark, France, French Polynesia, Germany, Guatemala, Honduras, Hungary, India,  Ireland, Italy, Japan, Korea, Luxembourg, Malaysia, Malta, Mexico, Mongolia,  Netherlands, New Caledonia, New Zealand, Oman, Panama, Paraguay, Poland, Puerto  Rico, Romania, Russian Federation, South Africa, Spain, Sweden, Switzerland, Taiwan,  Trinidad and Tobago, United Arab Emirates, and the United Kingdom.",
      "recall_number": "Z-0978-2020",
      "product_description": "Universa Soft Ureteral Stent, Global Product No. G49887  G49933  G49934  G49937  G49940  G49941  G49942  G49945  G49947  G49948  G49949  G49950  G49951  G49953  G49955  G49956  G49957  G49958  G49959  G49961  G53145  G53676  G53677  G53687  G53689  G53692  G53693  G53694  G53703  G53706  G53711  G53723  G53724  G53725  G53726",
      "product_quantity": "13388 total",
      "reason_for_recall": "The wire guide may be incorrectly loaded into the wire guide holder, leading to the stiff tip of the wire guide being introduced into the patient instead of the flexible tip.",
      "recall_initiation_date": "20190104",
      "center_classification_date": "20200204",
      "termination_date": "20200529",
      "report_date": "20200212",
      "code_info": "8078013  8172113  8001369  8183381  NS7994828  8147249  8417607  8600625  NS8417608  NS7990886  7990888  8594598  8594599  8056338  8018675  8056337  8629502  NS8018677  NS8053511  NS8417612  NS8011064  NS8417614  NS8417615  7998415  8147267  8187145  8008415  8011065  8078026  8008416  8078027  8078028  8150465  8180873  8008417  8033600  8427840  8427841  8507952  8507953  8507954  8507955  7990900  8003104  NS7990899  7998422  7998423  8047039  8056331  8066970  8066972  8066973  8066974  8147295  8147296  8421552  8427843  8427847  8594610  7994831  8008426  8056327  8066976  8066977  8207795  8629522  NS8026827  NS8030272  NS8421563  NS8421564  NS8421566  NS8421567  8599661  8421568  NS8599665  NS8060481  NS8033606  NS8629506  NS8629507  NS8008428  NS8421571  NS8421572  NS8599666  NS8599667  NS8147321  NS8421573  NS8008429"
    }
  ]
}