{
  "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": [
    {
      "country": "United States",
      "city": "Memphis",
      "address_1": "1800 Pyramid Place",
      "reason_for_recall": "The retaining tabs component of the Set Screw Retaining Drive may be oversized, which will not allow proper mating between the Set Screw Retaining Drive and the set screw.",
      "address_2": "",
      "product_quantity": "7 units",
      "code_info": "TI13J01811",
      "center_classification_date": "20140130",
      "distribution_pattern": "US Distribution in the states of CA, NC, TX, IN, NJ, and MI.",
      "state": "TN",
      "product_description": "SET SCREW RETAINING DRIVER, REF 9010000820, QTY: 1 EA, Medtronic Sofamor Danek, USA, Inc.   Screwdriver - orthopedic manual surgical instrument.",
      "report_date": "20140205",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Medtronic Sofamor Danek USA Inc",
      "recall_number": "Z-0866-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "67203",
      "termination_date": "20140516",
      "more_code_info": "",
      "recall_initiation_date": "20140103",
      "postal_code": "38132",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}