{
  "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": "Chicago",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "69693",
      "recalling_firm": "Medacta Usa",
      "address_1": "1556 W Carroll Ave",
      "address_2": "N/A",
      "postal_code": "60607-1012",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Worldwide Distribution - US including CA, CO, ID and Internationally to Australia and Germany.",
      "recall_number": "Z-0225-2015",
      "product_description": "The MectaLIF Oblique Handle, model number 03.22.10.0262, is used to insert the MectaLIF oblique spinal cage implants.",
      "product_quantity": "32 oblique handles",
      "reason_for_recall": "The MectaLIF Oblique Handle has the laser marking "MEDIAL" on the incorrect side and could result in incorrect insertion of the device during surgery.",
      "recall_initiation_date": "20141021",
      "center_classification_date": "20141118",
      "termination_date": "20160314",
      "report_date": "20141126",
      "code_info": "Model Number: 03.22.10.0262;   Lot Number: 1314256"
    }
  ]
}