{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Lenexa",
      "address_1": "12076 Santa Fe Trail Dr",
      "reason_for_recall": "The firm is recalling the products due to a potential for false negative test results.",
      "address_2": "",
      "product_quantity": "493 of lot 082505; 529 of lot 131988; and 448 of lot 131994",
      "code_info": "Lots: 082505; 131988; 131994",
      "center_classification_date": "20130212",
      "distribution_pattern": "Worldwide Distribution - USA Nationwide and the countries Canada and the United Kingdom",
      "state": "KS",
      "product_description": "Remel Xpect Clostridium difficile Toxin A/B, IVD,  20 clostridium difficile toxin A/B tests, REF 24650.      Product Usage:  Usage:  The test kit is a rapid in vitro immunochromatographic test for the direct, qualitative detection of Clostridium difficile Toxin A and/or B in human fecal specimens. The test is intended for use as an aid in diagnosis of Clostridium difficile-associated disease.",
      "report_date": "20130220",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Remel Inc",
      "recall_number": "Z-0806-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "63558",
      "termination_date": "20130604",
      "more_code_info": "",
      "recall_initiation_date": "20120820",
      "postal_code": "66215-3519",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}