{
  "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": [
    {
      "status": "Terminated",
      "city": "Raynham",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79518",
      "recalling_firm": "DePuy Mitek, Inc., a Johnson & Johnson Co.",
      "address_1": "325 Paramount Dr",
      "address_2": "N/A",
      "postal_code": "02767-5199",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution in the states of OH, WA, CO",
      "recall_number": "Z-1749-2018",
      "product_description": "LATARJET EXPERIENCE Sharp Curved Ostetome    Product Usage:  The Latarjet EXPERIENCE Instability Shoulder Set is intended to provide to the orthopedic surgeon with a means of bone fixation and to assist in the management of reconstructive surgeries.",
      "product_quantity": "84",
      "reason_for_recall": "Reports of product loosening or coming unscrewed from the handle.",
      "recall_initiation_date": "20171222",
      "center_classification_date": "20180508",
      "termination_date": "20190716",
      "report_date": "20180516",
      "code_info": "16D01,16D02, 16K01, 17A01, 17B01, 17B02"
    }
  ]
}