{
  "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": "2026-09-10",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "192674",
      "product_res_number": "Z-1000-2022",
      "event_date_initiated": "2022-02-18",
      "event_date_created": "2022-04-22",
      "recall_status": "Open, Classified",
      "res_event_number": "89846",
      "product_code": "QJR",
      "product_description": "NeuMoDx Cartridge-For in vitro diagnostic use with NeuMoOx Molecular Systems\n with either of the following assays:\n NeuMoDx SARS CoV-2 Test Strip (REF 300800)\n NeuMoDx Flu A-B/RSV/SARS-CoV-2 Vantage Test Strip (REF 300900)\nNeuMoDx Laboratory Developed Tests (LDTs) for SARS-CoV-2 RNA detection\nNote: Results for targets other than SARS-CoV-2 are not impacted by this Urgent Medical Device Correction\nRef. Number: 100100",
      "code_info": "Lot Numbers: 115424, 115425, 115426, 115427, 115429, 115431.\n\nGTIN: 10814278020274",
      "firm_fei_number": "3010729479",
      "recalling_firm": "NeuMoDx Molecular Inc",
      "address_1": "1250 Eisenhower Pl",
      "city": "Ann Arbor",
      "state": "MI",
      "postal_code": "48108-3281",
      "additional_info_contact": "SAME\n734-477-0111",
      "reason_for_recall": "Potential for false positive results for SARS-CoV-2 in identified lots of cartridges, when used in conjunction with assays containing SARS-CoV-2 targets (NeuMoDx\" SARS-CoV-2 Test Strip Cat #300800 and NeuMoDx\" Flu A-B/RSV/SARS-CoV-2 Vantage Assay Cat #300900) result incorrect management of  patients",
      "root_cause_description": "Material/Component Contamination",
      "action": "QIAGEN issued customer Urgent Medical Device Correction notification via email firstly by English (then in local language if required)on 2/18/22. Letter states reason for recall, health risk and action to take: \n1. IMMEDIATELY discontinue use of the product and discard remaining inventory in accordance with your national and local safety and environmental regulations. Please contact QIAGEN Technical Service for a free-of-charge replacement of scrapped inventory.\n2. Share this Field Safety Corrective Action with all users of the NeuMoDx Cartridges in your facility to ensure they are aware of this notice.\n3. If you have already used NeuMoDx Cartridges from any of these lots in combination with the NeuMoDx SARS-CoV-2 Assay, the NeuMoDx Flu-A-B/RSV/SARS-CoV-2 Assay and NeuMoDx Laboratory Developed Tests (LDTs) for SARS-CoV-2 RNA detection please review all SARS-CoV-2 positive results to exclude erroneous diagnosis and treatment, except in those cases where alternative confirmation was obtained.\nNote: results for targets other than SARS-CoV-2 are not impacted by this Urgent Field Safety Corrective Action.\n4. Complete the attached response form and return to Quality.Communications@qiagen.com to confirm receipt of this notification.\n\nIf you have any questions regarding this notice, please contact QIAGEN Technical Services at 1-800-362-7737 or techservice-na@qiagen.com",
      "product_quantity": "773 (72 US and 701 ROW) cases (48 cartridges/case)",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution in the states of OH, MO, VA, MI, MI, FL, MD, IA, NY, MO and the countries of Italy, Germany, Switzerland, Sweden, Netherlands, Finland, Spain, United Kingdom, Belgium, Austria, Hong Kong, France, Denmark, Slovenia.",
      "openfda": {
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        "fei_number": [
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          "3012918440",
          "3004530258",
          "3016838963",
          "1119779",
          "3009875001",
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        ],
        "device_name": "Reagents, 2019-Novel Coronavirus Nucleic Acid",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "N"
      }
    }
  ]
}