{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Sunnyvale",
      "address_1": "904 E Caribbean Dr",
      "reason_for_recall": "Firm determined that some lots of CT/NG Swab 50 and CT/NG Urine collection kits contain a sub component with an expiry date that is earlier than the kit expiration date.",
      "address_2": "",
      "product_quantity": "729 kits US, 47 kits ROW.",
      "code_info": "Part number: CT/NGSWAB-50:  Lot numbers: 46A202C, 46A202D, 46A202E, 46A202F, 46A202G, Flock swab expires end of July 2015. Kit expires October 2015.  Lot numbers 26N121H, and 28N134D.- Cleaning swabs expire end of June 2016. Kits expires November 2016.",
      "center_classification_date": "20150820",
      "distribution_pattern": "Worldwide distribution.  US nationwide, including North Mariana Islands, Aruba, Canada, Chile, Colombia, Costa Rica, Cyprus, Guam, Guatemala, Italy, Malawi, Micronesia Federated States, Panama, San Marino, South Africa, Spain, Switzerland, and Zimbabwe.",
      "state": "CA",
      "product_description": "Xpert CT /NG Vaginal/Endocervical/ Specimen Collection Kit:  Part number CT/NGSWAB-50;    Microbiology: The Cepheid X pert CT /NG Vagina Endocervical/ Specimen Collection Kit is designed to collect, preserve and transport patient Chlamydia trachomatis and Neisseria gonorrhoeae DNA in endocervical and vaginal specimens from symptomatic and asymptomatic individuals prior to analysis with the Cepheid Xpert CT/NG Assay.",
      "report_date": "20150826",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Cepheid",
      "recall_number": "Z-2431-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "71841",
      "termination_date": "20150928",
      "more_code_info": "",
      "recall_initiation_date": "20150727",
      "postal_code": "94089-1189",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}