{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Trumbull",
      "state": "CT",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72107",
      "recalling_firm": "CooperSurgical, Inc.",
      "address_1": "75 Corporate Dr",
      "address_2": "N/A",
      "postal_code": "06611-1350",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to the states of : AL, AZ, CA, GA, IA, IL, KS, LA, MA, MD, MN, MO, MS, NY, OH, PA, TN, TX, VA, and VT.",
      "recall_number": "Z-0105-2016",
      "product_description": "CooperSurgical LEEP REDIKIT-Used as a surgical preparatory kit for Loop Electrosurgical Excision Procedure  P/N 6061",
      "product_quantity": "305 units",
      "reason_for_recall": "Kit Label incorrect :Labeled with Lidocaine HCI drug cartridges Lidocaine HCl (2%) but contains  vials Lidocaine HCl (1%)",
      "recall_initiation_date": "20150901",
      "center_classification_date": "20151006",
      "termination_date": "20160129",
      "report_date": "20151014",
      "code_info": "LOT 187889"
    }
  ]
}