{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Elyria",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89062",
      "recalling_firm": "Invacare Corporation",
      "address_1": "1200 Taylor St",
      "address_2": "N/A",
      "postal_code": "44035-6248",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Canada, Australia, Thailand, New Zealand.",
      "recall_number": "Z-0446-2022",
      "product_description": "Invacare AVIVA FX with LiNX Gyro Power Wheelchair  (with LiNX Gyro Module Model Numbers DLX-GRY100-A and DLX-GRY101-A)  Models: IFX-20R, IFX-20SP, IFX-20MP, IFX-20C",
      "product_quantity": "303 units US; 20 units OUS",
      "reason_for_recall": "Power Wheelchairs with a LiNX Gyro component running firmware version 6.1.2 can experience a more aggressive deceleration rate than the programmed rate due to the system following the incorrect deceleration profile, resulting in potential injury",
      "recall_initiation_date": "20211112",
      "center_classification_date": "20220103",
      "report_date": "20220112",
      "code_info": "LiNX Gyro firmware version 6.1.2  UDI-DI Numbers: IFX-20C  00841447111627  IFX-20MP  00841447111658  IFX-20R  00841447111634  IFX-20SP  00841447111641  IFX20WIDE  00841447111658"
    }
  ]
}