{
  "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": "Tempe",
      "state": "AZ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "68535",
      "recalling_firm": "Ability Dynamics LLC",
      "address_1": "2082 E University Dr",
      "address_2": "N/A",
      "postal_code": "85281-4632",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US (nationwide) and in the countries of Australia and Canada.",
      "recall_number": "Z-1825-2014",
      "product_description": "RUSH81 Prosthetic Foot     Product Usage:  Prosthetic foot for human use",
      "product_quantity": "175 units",
      "reason_for_recall": "Ability Dynamics is recalling RUSH81 Prosthetic Foot because the existing bolts may be bottomed out in the threaded hole and this could lead to bolt failure.",
      "recall_initiation_date": "20140602",
      "center_classification_date": "20140618",
      "termination_date": "20140922",
      "report_date": "20140625",
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      "more_code_info": ""
    }
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}