{
  "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": "2026-04-15",
    "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": "74932",
      "recalling_firm": "Clark Laboratories, Inc. (dba,Trinity Biotech USA)",
      "address_1": "2823 Girts Rd",
      "address_2": "N/A",
      "postal_code": "14701-9666",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution to US nationwide including California, and China (Hong Kong).",
      "recall_number": "Z-2782-2016",
      "product_description": "Trinity Biotech Captia Measles IgM, REF/Product Code 2326060,Test Kit for 96 Determinations, IVD",
      "product_quantity": "US: 6 kits, Foreign: 50 kits",
      "reason_for_recall": "The product lot failed to meet QC acceptance criteria during stability testing.   The Calibrator OD was dropping causing the positive control to be invalid (running high out of range).",
      "recall_initiation_date": "20160711",
      "center_classification_date": "20160912",
      "termination_date": "20170509",
      "report_date": "20160921",
      "code_info": "Lot Number 2326060-043, Expiration Date 31 May 2017",
      "more_code_info": ""
    }
  ]
}