{
  "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": "2026-04-08",
    "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": "80169",
      "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": "The products were distributed to the following US states:  AZ, CA, CO, CT, DC, FL, GA, IL, IN, KS, KY, LA, MD, MI, MN, MO, MS, MT, NC, ND, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, WA, WI, and WV.  The products were distributed to the following foreign countries:  Canada, China, Ireland, Spain.",
      "recall_number": "Z-2200-2018",
      "product_description": "RS TANDEM 5F DL XPP, Catalog Number 60M019881",
      "product_quantity": "7",
      "reason_for_recall": "A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens).",
      "recall_initiation_date": "20180510",
      "center_classification_date": "20180614",
      "termination_date": "20200513",
      "report_date": "20180620",
      "code_info": "UPN: H96560M0198811; Lot: 5299857"
    }
  ]
}