{
  "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": "2026-08-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "51883",
      "product_res_number": "Z-0822-2007",
      "event_date_initiated": "2007-03-28",
      "event_date_posted": "2007-05-23",
      "recall_status": "Terminated",
      "event_date_terminated": "2008-09-08",
      "res_event_number": "37843",
      "product_code": "GNX",
      "k_numbers": [
        "K062109"
      ],
      "product_description": "BinaxNOW Influenza A&B 10 Test KIT \nPart Number: 416-110  contains NP Swabs with '8995' labeled on the swab wrapper",
      "code_info": "Kit Lot Numbers: 023378, 023411, 023433, 023616, 024021, 024384, 024479, 024480, 024622 NP Swabs Lot Number: 8995",
      "firm_fei_number": "1221359",
      "recalling_firm": "Binax, Inc. dba IMPD",
      "address_1": "10 Southgate Rd",
      "city": "Scarborough",
      "state": "ME",
      "postal_code": "04074-8303",
      "additional_info_contact": "Jenny Fuchs\n207-730-5700",
      "reason_for_recall": "Tip of the foam swab could detach from the shaft causing injury to the patient.",
      "root_cause_description": "Other",
      "action": "Inverness Medical issued recall notification by letter on 3/28/07. Customers are instructed to discard the NP swabs provided in the kits. The firm will replace the NP swabs. In the meantime customers are to use the tests with nasal wash/aspirate samples (influenza) or nasal wash samples (RSV). Response letters are to be signed by customers and returned to Inverness Medical.",
      "product_quantity": "2688 kits",
      "distribution_pattern": "Nationwide and Japan.",
      "openfda": {
        "k_number": [
          "K971494",
          "K901493",
          "K893579",
          "K132352",
          "K924006",
          "K871231",
          "K131599",
          "K131804",
          "K802931",
          "K871233",
          "K843659",
          "K123182",
          "K884191",
          "K133411",
          "K131606",
          "K843660",
          "K131619",
          "K872958"
        ],
        "registration_number": [
          "3033507883",
          "3003750284",
          "3026664926",
          "2030538",
          "9615056",
          "3023228837",
          "8010096",
          "3043226252",
          "3012494290",
          "3002792284",
          "3014150341",
          "3013530901"
        ],
        "fei_number": [
          "3033507883",
          "3003750284",
          "3026664926",
          "3006224287",
          "3023228837",
          "1000186023",
          "1000520007",
          "3043226252",
          "3012494290",
          "3002792284",
          "3014150341",
          "3013530901"
        ],
        "device_name": "Antigens, Cf (Including Cf Control), Influenza Virus A, B, C",
        "medical_specialty_description": "Microbiology",
        "regulation_number": "866.3330",
        "device_class": "1"
      }
    }
  ]
}