{
  "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,
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    }
  },
  "results": [
    {
      "cfres_id": "30939",
      "product_res_number": "Z-0373-04",
      "event_date_initiated": "2003-12-15",
      "event_date_posted": "2004-07-20",
      "recall_status": "Terminated",
      "event_date_terminated": "2004-06-21",
      "res_event_number": "27995",
      "product_code": "GQG",
      "k_numbers": [
        "K022133"
      ],
      "product_description": "Directigen (TM) EZ RSV In-Vitro Diagnostic test kit, containing reagents and controls for 30 tests, packaged in papercard carton. Catalog #256030.",
      "code_info": "lots 3253709, exp 12/18/03 and 3289760, exp 2/20/04",
      "firm_fei_number": "1119779",
      "recalling_firm": "Becton Dickinson & Co.",
      "address_1": "7 Loveton Cir",
      "city": "Sparks",
      "state": "MD",
      "postal_code": "21152-9212",
      "additional_info_contact": "Ms. Jody Hoffmann\n410-316-4098",
      "reason_for_recall": "Diagnostic test kit may exhibit false positive results.",
      "root_cause_description": "Other",
      "action": "The recalling firm notified consignees by fax, e-mail and letters 12/15/03. The letter advised of the false positive test results and requested end users to discontinue use and discard remaining packages for replacement. Consignees were requested to return response form.",
      "product_quantity": "600 kits",
      "distribution_pattern": "Product was sold to 242 direct account end users nationwide and 2 affiliated distributors in foreign countries.",
      "openfda": {
        "k_number": [
          "K854081",
          "K874127",
          "K882277",
          "K853695",
          "K802936",
          "K253318",
          "K133140",
          "K882629",
          "K070747",
          "K132456",
          "K770804",
          "K964870",
          "K032166",
          "K022845",
          "K162911",
          "K884516",
          "K843673",
          "K101918",
          "K022133",
          "K121633",
          "K021789",
          "K041445",
          "K240280",
          "K021687",
          "K896097",
          "K101514",
          "K862429",
          "K091235",
          "K023779",
          "K130398",
          "K862743",
          "K770808"
        ],
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        ],
        "device_name": "Antigen, Cf (Including Cf Controls), Respiratory Syncytial Virus",
        "medical_specialty_description": "Microbiology",
        "regulation_number": "866.3480",
        "device_class": "1"
      }
    }
  ]
}