{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "73236",
      "product_res_number": "Z-0212-2009",
      "event_date_initiated": "2008-07-02",
      "event_date_posted": "2008-11-03",
      "recall_status": "Terminated",
      "event_date_terminated": "2008-11-04",
      "res_event_number": "49385",
      "product_code": "GNX",
      "k_numbers": [
        "K023556"
      ],
      "product_description": "BioStar OIA FLU AB, Catalog 90007. Packaged 30 devices per tray. BioStar, Louisville, CO 80027",
      "code_info": "Lot # 193130DA Lot trace: 193198, 193198-2, 193199, 193199-2, 194062, 194062-2.",
      "firm_fei_number": "1720655",
      "recalling_firm": "Inverness Medical BioStar Inc.",
      "address_1": "331 S 104th St",
      "city": "Louisville",
      "state": "CO",
      "postal_code": "80027-9713",
      "additional_info_contact": "207-730-5740",
      "reason_for_recall": "Diagnostic kits for flu were distributed with incorrect components.",
      "root_cause_description": "Mixed-up of materials/components",
      "action": "Consignees were notified by a Important Customer Notification letter on 7/2/2008 and told to re-examine patient records that indicated a negative result and to destroy any remaining recalled product.  The accompanying record should be filled out and faxed to Technical Service.  If consignees further distributed any kits, they were to forward the notification to these accounts to assure that patient results were reviewed, and destruction of remaining kits could be verified.  For assistance, customers can call 800-637-3717.",
      "product_quantity": "509 kits",
      "distribution_pattern": "Nationwide Distribution --- including state of IL.",
      "openfda": {
        "k_number": [
          "K131599",
          "K123182",
          "K131804",
          "K901493",
          "K871233",
          "K924006",
          "K802931",
          "K133411",
          "K131619",
          "K871231",
          "K131606",
          "K843660",
          "K872958",
          "K132352",
          "K884191",
          "K893579",
          "K843659",
          "K971494"
        ],
        "registration_number": [
          "3026664926",
          "3014150341",
          "3013530901",
          "3033507883",
          "3003750284",
          "3023228837",
          "3012494290",
          "2030538",
          "3002792284",
          "9615056",
          "8010096",
          "3043226252"
        ],
        "fei_number": [
          "3026664926",
          "3014150341",
          "3013530901",
          "3033507883",
          "3003750284",
          "1000186023",
          "3012494290",
          "3023228837",
          "3006224287",
          "3002792284",
          "1000520007",
          "3043226252"
        ],
        "device_name": "Antigens, Cf (Including Cf Control), Influenza Virus A, B, C",
        "medical_specialty_description": "Microbiology",
        "regulation_number": "866.3330",
        "device_class": "1"
      }
    }
  ]
}