{
  "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": "Port Washington",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "94832",
      "recalling_firm": "Medical Depot Inc.",
      "address_1": "99 Seaview Blvd Fl 2",
      "address_2": "",
      "postal_code": "11050-4606",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Nationwide Foreign: Canada",
      "recall_number": "Z-2355-2024",
      "product_description": "Nitro Glide Knee Walker-offers users recovering from a below-the-knee injury the ability to remain mobile and glide through their daily activities.  Model: 791RD (Red)",
      "product_quantity": "667 units",
      "reason_for_recall": "The tiller separates from the base/front caster assembly. If the knee walker fails, a user may fall and sustain an injury",
      "recall_initiation_date": "20240614",
      "center_classification_date": "20240712",
      "report_date": "20240724",
      "code_info": "UPC: 822383019086 (791RD) All serial numbers beginning with  21S",
      "more_code_info": ""
    }
  ]
}