{
  "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": "Sugar Land",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85830",
      "recalling_firm": "TeDan Surgical Innovations LLC",
      "address_1": "12615 W Airport Blvd Ste 200",
      "address_2": "",
      "postal_code": "77478-6203",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide distribution - U.S. Nationwide distribution including in the states of: AZ, CA, FL, GA, HI, IL, MA, MI, NC, NH, NJ, NY, NV, PA, PR, TN, TX, and WA . The countries of  Australia, Canada, France, Philippines, Taiwan, U.A.E., and United Kingdom.",
      "recall_number": "Z-2525-2020",
      "product_description": "3COR DISTRACTION SCREW, 14 MM, STERILE, 5/BOX - Product Usage: intended to be used for distraction in the anterior approach to the cervical spine.",
      "product_quantity": "1935 screws (packaged into 387 boxes) - [5 screws per box]",
      "reason_for_recall": "Lack of pouch seal.  Product is labelled as sterile.",
      "recall_initiation_date": "20200515",
      "center_classification_date": "20200707",
      "termination_date": "20220908",
      "report_date": "20200715",
      "code_info": "Product Code: D-0014  UDI Number: 00843059121742  Lot Number:  2018020801  2018080601",
      "more_code_info": ""
    }
  ]
}