{
  "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": "Miami",
      "state": "FL",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72707",
      "recalling_firm": "Nipro Medical Corporation",
      "address_1": "3150 Nw 107th Ave",
      "address_2": "N/A",
      "postal_code": "33172",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Other",
      "distribution_pattern": "US distribution including TN.",
      "recall_number": "Z-0599-2016",
      "product_description": "NIPRO SafeTouch II Safety AVF Needle,  17G x 1 ¿ inch.  Item code FS+173230BC.",
      "product_quantity": "160,000 pieces.",
      "reason_for_recall": "Device has the potential to have torn wings.",
      "recall_initiation_date": "20140401",
      "center_classification_date": "20160106",
      "termination_date": "20161214",
      "report_date": "20160113",
      "code_info": "Model No.: FS+173230BC, Lot #14A22 and Lot #14A26."
    }
  ]
}