{
  "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-2053-2019",
      "product_description": "MOOG Curlin Infusion Administration Set, REF 340-4130, Non-DEHP Tubing with Non-Vented Bag Spike and Vented 0.2 Micron Filter, packaged 20 sets/carton, sterile.    Product Usage:  Administration set to be used with the Moog Curlin Infusion Pump. The pump can be used for intravenous, intra-arterial, epidural, subcutaneous, or enteral infusions.",
      "product_quantity": "569/20-set caess",
      "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 CF1819415, CF1820215, CF1821616, CF1822914, and CF1823615, UDI 38148440000464."
    }
  ]
}