{
  "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": "Naples",
      "state": "FL",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "75050",
      "recalling_firm": "Arthrex, Inc.",
      "address_1": "1370 Creekside Blvd",
      "address_2": "N/A",
      "postal_code": "34108-1945",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "OR, NY, MN, KY, CA, ID, CO, MA, and FL.  Thailand.",
      "recall_number": "Z-2918-2016",
      "product_description": "Arthrex Suture Washer",
      "product_quantity": "45 devices",
      "reason_for_recall": "The device was assembled incorrectly. Suture and washer were not assembled; components were placed loose in the package.",
      "recall_initiation_date": "20160812",
      "center_classification_date": "20160930",
      "termination_date": "20190820",
      "report_date": "20161012",
      "code_info": "Unique Device Identifier (UDI):  00888867118607;   Catalog # AR-7000-18T; Batch #10028617."
    }
  ]
}