{
  "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,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Sunnyvale",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93125",
      "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": "Worldwide distribution - US Nationwide and the countries of Costa Rica, Ireland, Estonia, United Kingdom, Germany, Italy, Greece, Poland, Switzerland, Hong Kong, United Arab Emirates.",
      "recall_number": "Z-0216-2024",
      "product_description": "Xpert Xpress Strep A, REF:Xprstrepa-CE-10, CE IVD,",
      "product_quantity": "1,413 kits ( 10 test per kit)",
      "reason_for_recall": "pipettes packaged in Strep A test may fail to dispense an adequate sample volume which could result in \"invalid\" results or no result test  results.",
      "recall_initiation_date": "20230424",
      "center_classification_date": "20231102",
      "report_date": "20231108",
      "code_info": "UDI: (01)07332940006297/ Lot: 23815"
    }
  ]
}