{
  "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": "Salt Lake City",
      "state": "UT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82864",
      "recalling_firm": "Zevex Incorporated (dba MOOG Medical Devices Group)",
      "address_1": "4314 S Zevex Park Ln",
      "address_2": "N/A",
      "postal_code": "84123-7881",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution was made to GA, IL, KS, MA, MI, and OH.  There was no foreign/military/government distribution.",
      "recall_number": "Z-2054-2019",
      "product_description": "MOOG Curlin Infusion Administration Set, REF 340-4130-V, Non-DEHP Tubing with Non-Vented Bag Spike and Vented 0.2 Micron Filter with add-on check valve, packaged 20 sets/carton, sterile.  The firm name on the label is ZEVEX, Inc., Salt Lake City, UT.",
      "product_quantity": "756/20-set cases",
      "reason_for_recall": "Administration sets leaked at the filter.",
      "recall_initiation_date": "20190227",
      "center_classification_date": "20190723",
      "termination_date": "20210428",
      "report_date": "20190731",
      "code_info": "Lot numbers CF1820216, CF1821617, CF1822214, and CF1823616, UDI 38148440000471."
    }
  ]
}