{
  "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": [
    {
      "country": "United States",
      "city": "Naples",
      "address_1": "1370 Creekside Blvd",
      "reason_for_recall": "Screws provided in the device package are 6 mm longer than intended.",
      "address_2": "",
      "product_quantity": "20 units",
      "code_info": "Product Code: AR-8545-20;  Batch Number: 10308261;  UDI: 00888867124424",
      "center_classification_date": "20200317",
      "distribution_pattern": "US distribution to MA, MN, ND, OH, SD, TN.      International distribution to Australia, Korea, China",
      "state": "FL",
      "product_description": "Low Profile Screw, 4.5 x 20 mm    The Low Profile ScrewTM, 4.5 x 20 mm, AR-8545-20, is used with the Ankle Fusion Line of plates and is intended to provide internal unicortical or bicortical bone fixation.",
      "report_date": "20200325",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Arthrex, Inc.",
      "recall_number": "Z-1510-2020",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "84030",
      "termination_date": "20210908",
      "more_code_info": "",
      "recall_initiation_date": "20191001",
      "postal_code": "34108-1945",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}