{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Addison",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82201",
      "recalling_firm": "CTL Medical Corporation",
      "address_1": "4550 Excel Pkwy Ste 300",
      "address_2": "N/A",
      "postal_code": "75001-5714",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "distributor and user level",
      "recall_number": "Z-1030-2019",
      "product_description": "CTL Medical Hex Driver, 1/4\" Square QC, 4.0 Ratcheting  Ref 015.7050",
      "product_quantity": "133 total devices",
      "reason_for_recall": "the anti-toggle ring of the hex driver may separate from the driver shaft. If this occurs during surgery, the anti-toggle ring can be pressed into the pedicle screw head and cause separation of the screw from the housing upon tightening.  if the anti-toggle ring remains in the pedicle crew head and can interfere with final tightening of the pedicle screw construct.  this can lead to failure of the set crew and relies of the rod from the construct.",
      "recall_initiation_date": "20180705",
      "center_classification_date": "20190320",
      "termination_date": "20210428",
      "report_date": "20190327",
      "code_info": "Lot 7EQAB-D, 7ATAB-D"
    }
  ]
}