{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Memphis",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87842",
      "recalling_firm": "Medtronic Sofamor Danek USA, Inc",
      "address_1": "4340 Swinnea Rd",
      "address_2": "N/A",
      "postal_code": "38118-6603",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "International distribution in the countries of France, Switzerland and Jordan. No US distribution.",
      "recall_number": "Z-1797-2021",
      "product_description": "Braive Growth Modulation System Break-Off Set Screws - Product Usage: intended to limit further progression of the spinal curvature and provide correction of the thoracic curve while allowing continued skeletal growth by compression of the convex side of the scoliotic curve.",
      "product_quantity": "162 UNITS",
      "reason_for_recall": "Product is impacted by a thread profile defect due to a manufacturing issue.",
      "recall_initiation_date": "20210427",
      "center_classification_date": "20210604",
      "termination_date": "20240820",
      "report_date": "20210616",
      "code_info": "CT20L012 and CT20L020.    CT20L012 EXP  2 DEC 2028  CT20L020 EXP 11 DEC 2028"
    }
  ]
}