{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Valencia",
      "state": "CA",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85660",
      "recalling_firm": "Utak Laboratories Inc",
      "address_1": "25020 Avenue Tibbitts",
      "address_2": "N/A",
      "postal_code": "91355-3447",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution. US nationwide, Canada, Australia, France, Germany, Israel, Italy, New Zealand, Philippines, and United Kingdom.",
      "recall_number": "Z-2407-2020",
      "product_description": "Utak NR Trace Elements Serum Control, 5 ml, REF 66816.  The responsible firm on the label is UTAK LABORATORIES, INC., Valencia, CA. Control for in vitro diagnostics.",
      "product_quantity": "1,395 vials",
      "reason_for_recall": "The product has an incorrect reference value for cadmium and an incorrect expected range.",
      "recall_initiation_date": "20200320",
      "center_classification_date": "20200622",
      "termination_date": "20200722",
      "report_date": "20200701",
      "code_info": "Lot C2540"
    }
  ]
}