{
  "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": "72697",
      "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 states of TX, OH, MI, and ME; and the countries of FR, DE, SK, IT, NL, CH, and CZ.",
      "recall_number": "Z-0657-2016",
      "product_description": "FMS neXtra¿ 3.5mm Aggressive Cutter Shaver Blades; Product Code: 283315    Intended to provide controlled cutting, shaving, and abrading of tissue during orthopedic procedures.",
      "product_quantity": "45 units",
      "reason_for_recall": "Product is incorrectly labeled. The blade configuration in the affected lots does not match the description on the label.",
      "recall_initiation_date": "20151120",
      "center_classification_date": "20160115",
      "termination_date": "20170412",
      "report_date": "20160127",
      "code_info": "Lot Number: M1505053",
      "more_code_info": ""
    }
  ]
}