{
  "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": {
      "skip": 0,
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  "results": [
    {
      "status": "Ongoing",
      "city": "Bridgend",
      "state": "N/A",
      "country": "United Kingdom",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92662",
      "recalling_firm": "ORTHO-CLINICAL DIAGNOSTICS",
      "address_1": "Felindre Meadows",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the country of Canada.",
      "recall_number": "Z-2358-2023",
      "product_description": "VITROS Immunodiagnostic Products Troponin I ES Calibrators",
      "product_quantity": "4,013 units",
      "reason_for_recall": "Reagent packs could potentially contain incorrect wells, which will generate incorrect, and potentially false negative, results.",
      "recall_initiation_date": "20230605",
      "center_classification_date": "20230808",
      "report_date": "20230816",
      "code_info": "Product Code: 6802302; UDI-DI: 10758750002511; Lot No.: 4800; Expiration Date: 10-Jun-2023."
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}