{
  "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": [
    {
      "country": "United States",
      "city": "Queensbury",
      "address_1": "603 Queensbury Ave",
      "reason_for_recall": "AngioDynamics became aware that Uni*Fuse Infusion Systems with Cooper Wire have the potential to contain an incorrect sized guidewire (too long).",
      "address_2": "",
      "product_quantity": "Domestic: 70 units; Foreign: 27 units",
      "code_info": "Lot 4731639 (exp. date 31-Mar-17)",
      "center_classification_date": "20140818",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) and Internationally to Austria, Australia, Ireland, Malaysia, Sweden, and Switzerland.",
      "state": "NY",
      "product_description": "Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE, 5F x 90 cm x 10 cm Infusion Pattern, Catalog No./REF 12401806, Product No. H787124018065, STERILE -- AngioDynamics, 603 Queensbury Avenue, Queensbury, NY 12804",
      "report_date": "20140827",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Angiodynamics, Inc.",
      "recall_number": "Z-2260-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "68980",
      "termination_date": "20170327",
      "more_code_info": "",
      "recall_initiation_date": "20140806",
      "postal_code": "12804-7619",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}