{
  "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": "2026-04-01",
    "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": "89675",
      "recalling_firm": "NeuMoDx Molecular Inc",
      "address_1": "1250 Eisenhower Pl",
      "address_2": "N/A",
      "postal_code": "48108-3281",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "N/A",
      "distribution_pattern": "US Nationwide distribution in the states of FL, MD, MI, NY.",
      "recall_number": "Z-0738-2022",
      "product_description": "NeuMoDx Flu A-B/RSV/SARS-CoV-2 Vantage Test Strip, Ref # 300900 (marketed under EUA202947).  Distributed in boxes of 6 assay strips in individual pouches.   Box, pouch and strips all labeled with product name, ref #, lot #, and expiration date.",
      "product_quantity": "102 boxes",
      "reason_for_recall": "A risk for product contamination was identified for the affected product lot. If used, there is an increased potential for SARS-CoV-2 false positive results when using the product.",
      "recall_initiation_date": "20220121",
      "center_classification_date": "20220308",
      "report_date": "20220316",
      "code_info": "Lot: 116305 S/L-02 (Sublot 02),UDI: 10814278020830"
    }
  ]
}