{
  "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 III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "75420",
      "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": "Letter",
      "distribution_pattern": "Nationwide Distribution to AL, AR, CA, FL, GA, IL, KY, LA, MI, MN, MO, NC, OH, OK, SC, NY, ME, PA, MD, VA, WA, WI, WV, TN, and TX",
      "recall_number": "Z-0775-2017",
      "product_description": "ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5 F Stiffened Micro-Introducer Kit, 45CM NT/T ECHO B PG, Item Number H787065970515, Catalog No.REF 06597051, 2)  5 F Stiffened Micro-Introducer Kit, 45CM NT/T ECHO S PG,  Item Number H787065970535, Catalog No.REF 06597053, 3) 5 F Stiffened Micro-Introducer Kit, 45CM NT/T ECHO A PG,  Item Number H787065970555, Catalog No.REF 06597055  Indicated for percutaneous introduction of guidewire or catheter into the vascular system following a small 21-gauge needle stick",
      "product_quantity": "996 boxes",
      "reason_for_recall": "Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator components has determined that the products listed in their September 7, 2016 Recall Notification have the potential for the rotating luer to detach from the dilator hub during use.  AngioDynamics has confirmed that affected sheath/dilators (Greatbatch Model Numbers 10904-001 and 10904-002) have been included in packaged AngioDynamics Stiffened Micro-Introducer Kits.",
      "recall_initiation_date": "20160928",
      "center_classification_date": "20161216",
      "termination_date": "20180618",
      "report_date": "20161228",
      "code_info": "Batch/Lot: 1) 5030537, 5037976, 5043444, 5059984, 5066413, 2) 5024545, 5031723, 5038659, 5042534, 5065538, 5071294, 5076428, 5082169, 3) 5022318, 5032456, 5034279, 5081986, 5082446"
    }
  ]
}