{
  "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": [
    {
      "country": "United States",
      "city": "Durham",
      "address_1": "100 Rodolphe St",
      "reason_for_recall": "The VITEK¿ 2 Systems Software Version 9.01 software may display incorrect organism identification information as well as the associated Antimicrobial Susceptibility Testing (AST) results when using the VITEK¿ 2 FLEXPREP\" feature.",
      "address_2": "",
      "product_quantity": "five (5) VITEK¿ 2 Systems Software version 9.01",
      "code_info": "Product Description: KIT UPDT VTK2 9.01 EN,      UDI: 03573026561260",
      "center_classification_date": "20181219",
      "distribution_pattern": "Nationwide distribution to CO, IL, MO, TX.",
      "state": "NC",
      "product_description": "VITEK¿ 2 Systems Software Version 9.01 Update Kit.",
      "report_date": "20181226",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "bioMerieux, Inc.",
      "recall_number": "Z-0639-2019",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "81589",
      "termination_date": "20210707",
      "more_code_info": "",
      "recall_initiation_date": "20181113",
      "postal_code": "27712-9402",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}