{
  "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": "2026-03-18",
    "results": {
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      "city": "Austin",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
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      "recalling_firm": "Luminex Corporation",
      "address_1": "12212 Technology Blvd",
      "address_2": "N/A",
      "postal_code": "78727-6101",
      "voluntary_mandated": "Voluntary: Firm initiated",
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      "product_description": "ARIES SARS-CoV-2 Assay, REF: 50-10047",
      "product_quantity": "5,141 (24 Cassettes)",
      "reason_for_recall": "A part defect with the wash 1 syringe of an SARS-CoV-2 assay could lead to incomplete extraction thereby producing an invalid or false negative assay result.",
      "recall_initiation_date": "20220914",
      "center_classification_date": "20221026",
      "report_date": "20221102",
      "code_info": "Lot - Expiration:   AB4723A - 05/25/2022, AB5041A - 05/25/2022, AB5060A - 06/01/2022, AB5061A - 06/06/2022, AB5081A - 06/07/2022, AB5139A - 09/10/2022, AB5141A - 09/16/2022, AB5263A - 09/27/2022, AB5282A - 10/05/2022, AB6640A - 06/8/2023, AB6720A - 06/13/2023",
      "more_code_info": ""
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}