{
  "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": "Elyria",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "64044",
      "recalling_firm": "Invacare Corporation",
      "address_1": "1 Invacare Way",
      "address_2": "N/A",
      "postal_code": "44035-4190",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution including the states of CA & MT.",
      "recall_number": "Z-0785-2013",
      "product_description": "Solara 3G Custom Manual Wheelchair      Product Usage: To provide mobility to a person restricted to a sitting position.",
      "product_quantity": "3 units",
      "reason_for_recall": "The potential exists for the wheel to rotate freely despite engagement of hub brake.",
      "recall_initiation_date": "20120910",
      "center_classification_date": "20130204",
      "termination_date": "20140513",
      "report_date": "20130213",
      "code_info": "Model #3G, Serial numbers: 12GE003750, 12GE003554 and 12HE001766.",
      "more_code_info": ""
    }
  ]
}