{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Wien",
      "state": "N/A",
      "country": "Austria",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71950",
      "recalling_firm": "Otto Bock Healthcare Product",
      "address_1": "Brehmstrasse 16",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Distributed to the state OH.",
      "recall_number": "Z-2438-2015",
      "product_description": "Otto Bock Healthcare Products GmbH Genium X3  Model Number: 3B5-2, Manufacturer Otto Bock Healthcare Products GmbH.     Intended to be used solely for lower limb prosthetic fittings.",
      "product_quantity": "1",
      "reason_for_recall": "Otto Bock Healthcare Products GmbH is recalling the new Genium X3 knee joint prosthesis due to issues with the resistance-control of the hydraulics, which may fail under conditions.",
      "recall_initiation_date": "20150812",
      "center_classification_date": "20150821",
      "termination_date": "20151028",
      "report_date": "20150902",
      "code_info": "Serial Number 201528049, manufactured on 01 July 2015"
    }
  ]
}