{
  "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": "Durham",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90605",
      "recalling_firm": "bioMerieux, Inc.",
      "address_1": "100 Rodolphe St",
      "address_2": "",
      "postal_code": "27712-9402",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "",
      "distribution_pattern": "International distribution to the countries of Estonia, Bahrain, Pakistan, UK, Singapore, Saudi Arabia, Thailand, and Vietnam.",
      "recall_number": "Z-1640-2022",
      "product_description": "VITEK 2 / MYLA    VITEK 2 Software versions 8.01, 8.02 (veterinary use only), 9.01, 9.02, 9.03  MYLA Software versions V4.8 and V4.9",
      "product_quantity": "",
      "reason_for_recall": "There are 7 reported software anomalies that may affect use of the device.",
      "recall_initiation_date": "20220713",
      "center_classification_date": "20220826",
      "report_date": "20220907",
      "code_info": "VITEK 2 Software Versions 8.01, 8.02 (veterinary only), 9.01, 9.02, 9.03 / MYLA Software Versions V4.8, V4.9  UDI/GTIN: 03573026553968, 03573026619060, 03573026609399, 03573026613914,  03573026619244, 03573026621568",
      "more_code_info": ""
    }
  ]
}