{
  "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": "2026-04-01",
    "results": {
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  "results": [
    {
      "status": "Terminated",
      "city": "Jamestown",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87637",
      "recalling_firm": "Clark Laboratories, Inc.",
      "address_1": "2823 Girts Rd",
      "address_2": "N/A",
      "postal_code": "14701-9666",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution and the country of Ireland.",
      "recall_number": "Z-1503-2021",
      "product_description": "Trinity Biotech Captia Measles IgM Kit, Catalog No. 2326060 - Product Usage: intended for the qualitative detection of Measles igM antibodies in human serum of patients suspected of measles (rubeola) infection.",
      "product_quantity": "80 kits",
      "reason_for_recall": "Positive Control may run high out of its assigned ISR range and result in an invalid run and necessitate retesting",
      "recall_initiation_date": "20210317",
      "center_classification_date": "20210427",
      "termination_date": "20220629",
      "report_date": "20210505",
      "code_info": "Kit Lot:  2326060-060  Expiration Date: 2021-06-28  (UDI): 05391516743655",
      "more_code_info": ""
    }
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}