{
  "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,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Hazelwood",
      "state": "MO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91148",
      "recalling_firm": "Biomerieux Inc",
      "address_1": "595 Anglum Rd",
      "address_2": "N/A",
      "postal_code": "63042-2320",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-0789-2023",
      "product_description": "VITEK 2 REAGENT YST TEST KIT VTK2 20 CARDS,  CATALOG 21343",
      "product_quantity": "14 units",
      "reason_for_recall": "As the temperature and time out of range was exceeded, product performances cannot be guaranteed",
      "recall_initiation_date": "20221109",
      "center_classification_date": "20230104",
      "report_date": "20230111",
      "code_info": "UDI/DI 03573026131937, Batch Numbers:  2432261103"
    }
  ]
}