{
  "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": "Naples",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82009",
      "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": "Worldwide Distribution: US (nationwide) to states of: AL, AZ, CA, CO, DC, FL, GA, HI, IA, ID, IL, KY, LA, MA, MD, MI, MN, MO, NC, ND, NH, NY, OH, OK, PA, RI, SC, SD, TN, TX, VA, WA, WI, and WY; and to countries of: Germany, Brazil and Australia.",
      "recall_number": "Z-1206-2019",
      "product_description": "Arthrex Burr, Oval, 12 Flute, 5.5 mm x 13 cm (AR-8550OBT)    These devices are indicated for resection of soft and osseous tissues in both large and small articular cavities during arthroscopic procedures.",
      "product_quantity": "2324",
      "reason_for_recall": "Devices may generate excessive heat during use.",
      "recall_initiation_date": "20190114",
      "center_classification_date": "20190423",
      "termination_date": "20230831",
      "report_date": "20190501",
      "code_info": "Lot Numbers: 10211276 (expiration date: 4/30/2023  and 10202784 (expiration date: 3/31/2023"
    }
  ]
}