{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Sunnyvale",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97911",
      "recalling_firm": "Cepheid",
      "address_1": "904 E Caribbean Dr",
      "address_2": "N/A",
      "postal_code": "94089-1189",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution and Puerto Rico.",
      "recall_number": "Z-0724-2026",
      "product_description": "Xpert MTB/RIF. Model Number: GXMTB/RIF-US-10.",
      "product_quantity": "9,880 units",
      "reason_for_recall": "Product testing did not meet expected stability criteria.",
      "recall_initiation_date": "20251105",
      "center_classification_date": "20251126",
      "report_date": "20251203",
      "code_info": "Model Number: GXMTB/RIF-US-10. UDI-DI: 07332940000912. Batch: 1000812229. Lot: 41302. Expiration Date: 2025-02-02",
      "more_code_info": ""
    }
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}