{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Ann Arbor",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90275",
      "recalling_firm": "NeuMoDx Molecular Inc",
      "address_1": "1250 Eisenhower Pl",
      "address_2": "",
      "postal_code": "48108-3281",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Domestic distribution to FL, NY, MD, PA, VA, MI, TN, NM. Foreign distribution to AT, AU, BE, CH, DE, FI, FR, GB, GR, HK, ID, IT, LT, NL, SA, SE, and SI.",
      "recall_number": "Z-1251-2022",
      "product_description": "NeuMoDx Flu A-B/RSV/SARS-CoV-2 Vantage Test Strip, Model No. 300900",
      "product_quantity": "459 kits US; 1626 kits OUS",
      "reason_for_recall": "There is a potential for reduced analytical sensitivity for samples in the 1x - 3x LOD range for Flu A, RSV, and SARS-CoV-2 targets. This may lead to false negative results, allowing ongoing transmission to others and delaying appropriate treatment.",
      "recall_initiation_date": "20220513",
      "center_classification_date": "20220608",
      "report_date": "20220615",
      "code_info": "UDI-DI (GTIN): 10814278020830  Cartridge lot numbers 111915 - 117508",
      "more_code_info": ""
    }
  ]
}