{
  "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": "Santa Clarita",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83563",
      "recalling_firm": "TriMed Inc.",
      "address_1": "27533 Avenue Hopkins",
      "address_2": "N/A",
      "postal_code": "91355-3910",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution was made to CA, FL, MD, TX, and WA.  There was military and foreign distribution was made to Australia.  There was no government distribution.",
      "recall_number": "Z-0118-2020",
      "product_description": "TriMed Dorsal Wrist Hook Plate, Dorsal, 4-Hole, REF WHD-4, contained in a tray, insert, or poly package containing varying amounts, Nonsterile, Single Use Only, Rx.  The firm name on the label is TriMed, Santa Clarita, CA.",
      "product_quantity": "5 devices",
      "reason_for_recall": "Modifications to the specification were not appropriately qualified through the company's design control process which may result in structural integrity issues of the device.",
      "recall_initiation_date": "20180824",
      "center_classification_date": "20191010",
      "termination_date": "20210428",
      "report_date": "20191016",
      "code_info": "Lot numbers 28884, 28885, 28886, and 28887"
    }
  ]
}