{
  "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 II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "69636",
      "recalling_firm": "CooperSurgical, Inc.",
      "address_1": "75 Vista Pl",
      "address_2": "N/A",
      "postal_code": "06611-3934",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA (Nationwide) and Internationally to  Canada, Portugal, and Hong Kong.",
      "recall_number": "Z-0484-2015",
      "product_description": "CooperSurgical LEEP RADIUS LOOP ELECTRODE (W 2.0 cm x D 1.0 cm D, 12 cm shaft ). Box of 5  Model Number(s): R2010  Intended Use: Diagnosis and treatment of non-invasive HPV-related or unrelated lesions of the lower genital tract.",
      "product_quantity": "595 units",
      "reason_for_recall": "Outer box is mislabeled as P/N R2010- Large Radius Loop Electrode instead of P/N R1010- Medium Radius Loop Electrode",
      "recall_initiation_date": "20141027",
      "center_classification_date": "20141127",
      "termination_date": "20150529",
      "report_date": "20141203",
      "code_info": "Lot 159621  Exp Date: 2017-05",
      "more_code_info": ""
    }
  ]
}