{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Blue Ash",
      "address_1": "4545 Creek Rd",
      "reason_for_recall": "There is a risk that the pinion gear in the device could fail under extreme use cases.",
      "address_2": "",
      "product_quantity": "792 units",
      "code_info": "N91U0W, N91U0X, N91L2P, N91N1J, and N91N2G",
      "center_classification_date": "20170531",
      "distribution_pattern": "Worldwide distribution.  The previously recalled products were distributed to the following countries: China, Japan, Singapore, and South Korea.",
      "state": "OH",
      "product_description": "Endopath ETS-FLEX Endoscopic Articulating Linear Cutter, VASCULAR/THIN 35MM",
      "report_date": "20170607",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Ethicon Endo-Surgery Inc",
      "recall_number": "Z-2174-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "76921",
      "termination_date": "20180503",
      "more_code_info": "",
      "recall_initiation_date": "20170331",
      "postal_code": "45242-2803",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}