{
  "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": "2026-04-08",
    "results": {
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      "city": "Jamestown",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81488",
      "recalling_firm": "Clark Laboratories, Inc. (dba,Trinity Biotech USA)",
      "address_1": "2823 Girts Rd",
      "address_2": "",
      "postal_code": "14701-9666",
      "voluntary_mandated": "Voluntary: Firm initiated",
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      "distribution_pattern": "IL, WV, NJ, AZ, MD, UT",
      "recall_number": "Z-0620-2019",
      "product_description": "ultra2 Genesys Variants Analyzer, REF 03-01-0045 intended to be used with automated high performance liquid chromatography (HPLC) systems employing ion exchange chromatography. For in vitro diagnostic use only.",
      "product_quantity": "14 devices",
      "reason_for_recall": "lack of 510K",
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      "center_classification_date": "20181218",
      "termination_date": "20220621",
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      "code_info": "all serial numbers",
      "more_code_info": ""
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}