{
  "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": "Chatsworth",
      "state": "CA",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "62555",
      "recalling_firm": "Iris Diagnostics",
      "address_1": "9172 Eton Ave",
      "address_2": "N/A",
      "postal_code": "91311-5805",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution",
      "recall_number": "Z-2124-2012",
      "product_description": "IRISpec\" CA/CB two-part urine chemistry control twin set, Iris Diagnostics part number 800-0074.    Intended Use: IRISpec\u001d CA/CB is an assayed QC material for monitoring of the urine chemistry analytes and devices as listed on the package insert.  For in vitro diagnostic (IVD) use only.",
      "product_quantity": "862",
      "reason_for_recall": "The firm recalled after it received complaints of IRISpec CA/CB two part Urine Chemistry Control, 101131-12, where the nitrite results read negative for the part B control, which should be positive.",
      "recall_initiation_date": "20120709",
      "center_classification_date": "20120801",
      "termination_date": "20140127",
      "report_date": "20120808",
      "code_info": "Iris Diagnostics part number 800-0074, lot number 131-12."
    }
  ]
}