{
  "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": "2026-04-15",
    "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": "24 units",
      "code_info": "Lot # - CA14C107",
      "center_classification_date": "20150112",
      "distribution_pattern": "US Distribution to the states of : CA, KS, KY, NC, TX, WA, MI, OH, IA, PA, OR, MS, FL, NY, GA and AR.",
      "state": "TN",
      "product_description": "POWEREASE Instruments Set Screw Breakoff Instrument, REF 2346010, Medtronic Sofamor Danek, USA, Inc.  Spinal surgical instrumrent.",
      "report_date": "20150121",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Medtronic Sofamor Danek USA Inc",
      "recall_number": "Z-0952-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "70032",
      "termination_date": "20150924",
      "more_code_info": "",
      "recall_initiation_date": "20141203",
      "postal_code": "38132",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}