{
  "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": "Irvine",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "67818",
      "recalling_firm": "Branan Medical Corporation",
      "address_1": "140 Technology Dr Ste 400",
      "address_2": "N/A",
      "postal_code": "92618-2426",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution: US (nationwide) and country of Canada.",
      "recall_number": "Z-1508-2014",
      "product_description": "ToxCup Drug Screen Cup, Catalogue Numbers: HT15, HT15A, PT11, PT11A, PT15A, PT23A,  a screening device for the detection of drugs and drug metabolites in human urine. For in vitro diagnostic use only.",
      "product_quantity": "9,800 units",
      "reason_for_recall": "May be labeled with incorrect result interpretation graphics on the ToxCup lid label.",
      "recall_initiation_date": "20140326",
      "center_classification_date": "20140424",
      "termination_date": "20140723",
      "report_date": "20140430",
      "code_info": "Lot Numbers:  O0056  O0067  N0854  O0013  O0099  O0100  O0057  O0059  O0060  O0079",
      "more_code_info": ""
    }
  ]
}