{
  "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": "Jamestown",
      "state": "NY",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "62440",
      "recalling_firm": "Clark Laboratories, Inc. (dba,Trinity Biotech USA)",
      "address_1": "2823 Girts Road",
      "address_2": "N/A",
      "postal_code": "14701",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution-including Puerto Rico and the states of AL, CA, IL, IN, MA, MD, NJ, OH, PA, TN, TX.",
      "recall_number": "Z-2445-2012",
      "product_description": "Trinity Biotech, Captia VZV IgG. Product code 2325600: 96 Tests; product code: 2325601: 480 tests.     For in vitro diagnostic use. Intended for the detection and quantitative determination of IgG antibody to VZV in human sera.",
      "product_quantity": "810 kits",
      "reason_for_recall": "The Positive Control for the Captia Varicella-Zoster Virus (VZV) IgG Kit has been reported as running high out of its assigned ISR range.",
      "recall_initiation_date": "20120529",
      "center_classification_date": "20120924",
      "termination_date": "20160524",
      "report_date": "20121003",
      "code_info": "Kit lot codes: 2325600-566, 2325601-566, 2325600-567, 2325601-567, 2325600-568",
      "more_code_info": ""
    }
  ]
}