{
  "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": "Raynham",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72703",
      "recalling_firm": "DePuy Mitek, Inc., a Johnson & Johnson Co.",
      "address_1": "325 Paramount Drive",
      "address_2": "N/A",
      "postal_code": "02767-5199",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US Distribution to the states of : AL, CA, CT, FL, KY, MN, MS, ND, NJ, NM and TX., and to the countries of: France, Netherlands and Norway.",
      "recall_number": "Z-0479-2016",
      "product_description": "VAPR¿ TRIPOLAR 90\" Degree Suction Electrodes (Model/Catalog No: 225028)",
      "product_quantity": "127",
      "reason_for_recall": "Mitek identified that on VAPR Tripolar 90 Degree Suction Electrode the ablation and coagulation buttons are colored incorrectly. The wiring for each button function was confirmed as correct and the non-conformance impacted button color only",
      "recall_initiation_date": "20151123",
      "center_classification_date": "20151223",
      "termination_date": "20170412",
      "report_date": "20151230",
      "code_info": "U1509202 and U1509162"
    }
  ]
}