{
  "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-0447-2022",
      "product_description": "Invacare AVIVA Storm RX with LiNX Gyro Power Wheelchair (with LiNX Gyro Module Model Numbers DLX-GRY100-A and DLX-GRY101-A)  Models: SRX-20R, SRX-20SP, SRX-20MP",
      "product_quantity": "1 unit US",
      "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: SRX-20MP  00841447114581  SRX-20R  00841447114604  SRX-20SP  00841447114598"
    }
  ]
}