{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Queensbury",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79193",
      "recalling_firm": "Angiodynamics, Inc.",
      "address_1": "603 Queensbury Ave",
      "address_2": "N/A",
      "postal_code": "12804-7619",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Distribution to the states of : AL, CA, CT, FL, GA, IL, IN, MD, MI, MN, MO, OH, OR, TX.",
      "recall_number": "Z-0742-2018",
      "product_description": "Soft-Vu Omni Flush Angiographic Catheter (UPN H787107322015); SV OF 5F x 65 cm .035 NB PG; Catalog Number: 10732201    AngioDynamics Angiographic Catheters are for use where angiographic diagnosis is indicated.",
      "product_quantity": "28",
      "reason_for_recall": "Product was placed into distribution prior to completion of all required post sterilization release activities.",
      "recall_initiation_date": "20170922",
      "center_classification_date": "20180227",
      "termination_date": "20180919",
      "report_date": "20180307",
      "code_info": "Lot Number: 5229642; Manufactured 6-Sep-17; Expiration Date: 31-Aug-20"
    }
  ]
}