{
  "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,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Fort Collins",
      "address_1": "320 E Vine Dr Ste 312",
      "reason_for_recall": "The dowel pin could potentially slip out of its press fit, resulting in the product potentially slumping to one side which could cause the patient to stumble.",
      "address_2": "",
      "product_quantity": "239",
      "code_info": "Product Part Number 16100. Serial Numbers 100200-101068, except for serial numbers within this range not released into final inventory for other reasons.",
      "center_classification_date": "20161215",
      "distribution_pattern": "Worldwide Distribution -- USA and Canada.",
      "state": "CO",
      "product_description": "IVEA 500A    Intended for Med-Surg patient care.",
      "report_date": "20161221",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Firefly Medical, Inc.",
      "recall_number": "Z-0767-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "75571",
      "termination_date": "20170801",
      "more_code_info": "",
      "recall_initiation_date": "20161101",
      "postal_code": "80524-2332",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}