{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Blue Ash",
      "address_1": "4545 Creek Rd",
      "reason_for_recall": "Use of the product with insufficient lubrication may prolong surgery due to trocar replacement. In addition, insufficient lubrication could result in a remote chance of introducing a minute particle if repeated insertions of the obturator or laparoscopic device damage the seal.",
      "address_2": "",
      "product_quantity": "1500",
      "code_info": "Lots P4TD1E  R4001U  R4052P",
      "center_classification_date": "20180515",
      "distribution_pattern": "Nationwide domestic distribution, including PR. International distribution to Saudi Arabia, United Arab Emirates, Belgium, Singapore, Taiwan, South Korea, Canada, Chile, Mexico, Japan, and Argentina.",
      "state": "OH",
      "product_description": "5mm Endopath Xcel with Optiview Technology, Bladeless Trocar with Stability Sleeve, 5mm, 150mm shaft length, 2B5XT",
      "report_date": "20180523",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Ethicon Endo-Surgery Inc",
      "recall_number": "Z-1887-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "79801",
      "termination_date": "20200408",
      "more_code_info": "",
      "recall_initiation_date": "20180326",
      "postal_code": "45242-2803",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}