{
  "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": "Glens Falls",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81477",
      "recalling_firm": "Angiodynamics Inc. (Navilyst Medical Inc.)",
      "address_1": "10 Glens Falls Tech Park",
      "address_2": "N/A",
      "postal_code": "12801-3864",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed to accounts in Florida. Foreign distribution to Great Britain.",
      "recall_number": "Z-0595-2019",
      "product_description": "Xcela Power Injectable PICC with PASV (XCELA PASV 4F SL 55CM Catheter Kit CE PG), Cat no. 55-711",
      "product_quantity": "Box of 1 Units",
      "reason_for_recall": "Specific lots of Xcela Power Injectable and BioFlo PICCs are labelled with incorrect expiration dates. The labelled expiration date extends the shelf life of the product beyond the date supported by validation testing. Although the product under recall has not yet reached its validated expiry date, removal of the affected product is warranted to prevent use beyond the validated expiry date.",
      "recall_initiation_date": "20181016",
      "center_classification_date": "20181211",
      "termination_date": "20200626",
      "report_date": "20181219",
      "code_info": "Lot 5096448"
    }
  ]
}