{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Redondo Beach",
      "state": "CA",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80179",
      "recalling_firm": "Quantimetrix Corporation",
      "address_1": "2005 Manhattan Beach Blvd",
      "address_2": "N/A",
      "postal_code": "90278-1205",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to the state of : Kansas",
      "recall_number": "Z-2257-2018",
      "product_description": "Dropper Plus Point-of-Care Urinalysis Dipstick Control kit    The Quantimetrix Dropper Plus Point-of-Care Urinalysis Dipstick Control is intended as a control for urinalysis reagent strips, microalbumin, and creatinine by the listed test methods, and as a control for confirmatory tests such as K-CHECK and Ictotest reagent tablets, and for hCG methods.",
      "product_quantity": "20 kits",
      "reason_for_recall": "The kits contained an incorrect lot of Dropper Plus Level 1 vials",
      "recall_initiation_date": "20171221",
      "center_classification_date": "20180620",
      "termination_date": "20210127",
      "report_date": "20180627",
      "code_info": "Lot 44450E"
    }
  ]
}