{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
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  "results": [
    {
      "cfres_id": "49185",
      "product_res_number": "Z-0222-2007",
      "event_date_initiated": "2006-09-29",
      "event_date_posted": "2006-11-29",
      "recall_status": "Terminated",
      "event_date_terminated": "2007-03-13",
      "res_event_number": "36699",
      "product_code": "MJH",
      "k_numbers": [
        "K982238"
      ],
      "product_description": "NOW Legionella Urinary Antigen Test.  22  test kit. For In Vitro Diagnostic Use\nProduct Code: 852-000",
      "code_info": "Lot Number: 024448 Exp. Date: March 14, 2008",
      "firm_fei_number": "1221359",
      "recalling_firm": "Inverness Medical Professional Diagnostics",
      "address_1": "10 Southgate Rd",
      "city": "Scarborough",
      "state": "ME",
      "postal_code": "04074-8303",
      "additional_info_contact": "Jenny Fuchs\n207-730-5740",
      "reason_for_recall": "Mislabeled product: Outer kit label reads NOW Legionella Urinary Antigen Test, inside contains S. pneumonia test pouches",
      "root_cause_description": "Other",
      "action": "Binax Inc. DBA Inverness Medical notified consignees by letter on 09/29/06 advising users to return unused product and distributors to recall to the user level.",
      "product_quantity": "531 kits",
      "distribution_pattern": "Worldwide, including USA, Canada, EU, South Korea, Singapore",
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        "k_number": [
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        "device_name": "Legionella, Spp., Elisa",
        "medical_specialty_description": "Microbiology",
        "regulation_number": "866.3300",
        "device_class": "2"
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}