{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Nevele",
      "state": "N/A",
      "country": "Belgium",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97354",
      "recalling_firm": "mo-Vis BVBA",
      "address_1": "Biebuyckstraat 15D",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the state of TX.",
      "recall_number": "Z-2457-2025",
      "product_description": "IDM-MULTI-R. Electrical wheelchair component.",
      "product_quantity": "15 units",
      "reason_for_recall": "Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check and the wheelchair producing unintended movement upon power-up when the joystick is out of neutral.",
      "recall_initiation_date": "20250710",
      "center_classification_date": "20250902",
      "report_date": "20250910",
      "code_info": "Model No. PRSPS0016; UDI-DI: 05407008320850; Serial No. 1000 to 1690."
    }
  ]
}