{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Memphis",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89739",
      "recalling_firm": "Wright Medical Technology, Inc.",
      "address_1": "1023 Cherry Rd",
      "address_2": "N/A",
      "postal_code": "38117-5423",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US distribution to Florida, North Carolina, Ohio, and Texas",
      "recall_number": "Z-0853-2022",
      "product_description": "EasyFuse Dynamic Compression System Instrument Pack",
      "product_quantity": "176 packs",
      "reason_for_recall": "The drill and adjustable drill guide can jam/bind intraoperatively resulting in the drill guide breaking.",
      "recall_initiation_date": "20220310",
      "center_classification_date": "20220331",
      "termination_date": "20260401",
      "report_date": "20220406",
      "code_info": "Model Number FFSP1530, UDI: 00889797103565    Lot Codes (Expiration Date): 781853-110321 (11/03/2029) and 780395-112221 (12/03/2029)"
    }
  ]
}