{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Ann Arbor",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88099",
      "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": "Letter",
      "distribution_pattern": "Worldwide distribution.",
      "recall_number": "Z-1978-2021",
      "product_description": "NeuMoDx Cartridge, For In Vitro Diagnostic Use on the NeuMoDx 288 and NeuMoDx 96 Molecular Systems, Model Number 100100",
      "product_quantity": "620 cases (29,760 cartridges total)",
      "reason_for_recall": "There is a potential for false positive results when certain lots of cartridges are used in conjunction with specific assays.",
      "recall_initiation_date": "20210504",
      "center_classification_date": "20210629",
      "termination_date": "20220621",
      "report_date": "20210707",
      "code_info": "GTIN: 10814278020274;    Lot Numbers: 106629  106630  106631  106632"
    }
  ]
}