{
  "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": "Reykjavik",
      "state": "",
      "country": "Iceland",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70693",
      "recalling_firm": "Ossur H / F",
      "address_1": "Grjothals 5",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Worldwide distribution: US distribution in TN and country of: Austria.",
      "recall_number": "Z-1322-2015",
      "product_description": "The Rheo Knee bionic prosthetic is to be used exclusively for fittings of lower extremity amputations.  RHEO KNEE uses Artificial Intelligence to continuously adapt to the user\u0019s walking style and environment. The RHEO KNEE recognizes and responds immediately to changes in speed, load and terrain, restoring the user\u0019s ability to walk naturally, comfortably and confidently at any speed.",
      "product_quantity": "4715 units (2 units affected)",
      "reason_for_recall": "The firm is recalling Rheo Knee bionic prosthetic due to it being discovered during an internal audit of the service line that devices were released for distribution without fully going through the assembly process.",
      "recall_initiation_date": "20150226",
      "center_classification_date": "20150325",
      "termination_date": "20151120",
      "report_date": "20150401",
      "code_info": "Rheo 2 Item Number: RKN120007    Serial #\u0019s affected:    323056  321498",
      "more_code_info": ""
    }
  ]
}