{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Miami",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "65274",
      "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": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA and the countries of  Canada, Bolivia, Chile, Uruguay, Belize, Dominica, Honduras, Jamaica, Paraguay and Venezuela.",
      "recall_number": "Z-1834-2014",
      "product_description": "NIPRO Safe Touch Safety Scalp Vein Set",
      "product_quantity": "176,000 pieces",
      "reason_for_recall": "There is a possibility of a crack in the CP luer connector. The position of the crack is at the connection site of the CP luer connector and the tubing. The crack could cause or contribute to leakage of fluids.",
      "recall_initiation_date": "20130504",
      "center_classification_date": "20140619",
      "termination_date": "20150302",
      "report_date": "20140625",
      "code_info": "Product Code: PR+25G19, Lots #\u0019s 12H31H and 12I14H; Product Code: SPR+21G19, Lots #\u0019s 12I24 and 12J11; Product Code: PR-25G19, Lot # 12H27H; and PR-23G19, Lot # 12I12H.",
      "more_code_info": ""
    }
  ]
}