{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Port Washington",
      "address_1": "99 Seaview Blvd Fl 2",
      "reason_for_recall": "Tip crutch failure involving the bottom of the metal portion which comes in contact with ground",
      "address_2": "",
      "product_quantity": "123,125 pairs",
      "code_info": "Item #.: 1) 10400-1, 2) 10400-8, 3) 10401-1, 4) 10401-8, 5) 10402-1 & 6) 10402-8",
      "center_classification_date": "20160630",
      "distribution_pattern": "Nationwide Distribution",
      "state": "NY",
      "product_description": "Aluminum crutch under the following labels: 1) Aluminum crutch, adult, 1 pair per case, 2) Aluminum crutch, adult, 8 pairs per case, 3) Aluminum crutch, youth, 1 pair per case, 4) Aluminum crutch 8 pairs per case, 5) Aluminum crutch, tall adult, 1 pair per case & 6) Aluminum crutch, tall adult, 8 pairs per case",
      "report_date": "20160706",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Medical Depot Inc.",
      "recall_number": "Z-2101-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "73918",
      "termination_date": "20180613",
      "more_code_info": "",
      "recall_initiation_date": "20160217",
      "postal_code": "11050-4606",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}