{
  "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": "Latham",
      "address_1": "14 Plaza Dr",
      "reason_for_recall": "AngioDynamics is recalling one lot of Soft-Vu Angiographic catheters because one of the catheter pouches within the outer box may be mislabeled.",
      "address_2": "",
      "product_quantity": "7 boxes/35 units",
      "code_info": "Lot: 564325",
      "center_classification_date": "20120809",
      "distribution_pattern": "Worldwide distribution: USA (nationwide) including states of: CA, KS, MO, and NC and countries of:  Czech Republic and Switzerland.",
      "state": "NY",
      "product_description": "AngioDynamics Angiographic catheter --- Soft-Vu (JB-1) Non-braided. --- Size: 5F; Length: 100cm; designed to accept guidewire: .035 in. --- Catalog No. [REF]: 10734201. Packaged in boxes of 5 catheters each, with manufacturer listed as AngioDynamics, Inc., Queensbury, NY USA.    Intended use: angiographic diagnosis.",
      "report_date": "20120815",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Angiodynamics Worldwide Headquarters",
      "recall_number": "Z-2180-2012",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "62341",
      "termination_date": "20160210",
      "more_code_info": "",
      "recall_initiation_date": "20120615",
      "postal_code": "12110-2166",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}