{
  "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": "2026-07-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Hazelwood",
      "state": "MO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99213",
      "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": "Letter",
      "distribution_pattern": "International distribution to the countries of Belgium and the Netherlands.",
      "recall_number": "Z-2715-2026",
      "product_description": "VITEK 2 AST-N447 TEST KIT  Product reference 424620",
      "product_quantity": "45,900 cards",
      "reason_for_recall": "Potential for false resistant carbapenem and/or cephalosporin results when analyzing samples with kits from affected lot that have pouch foil fractures.",
      "recall_initiation_date": "20260604",
      "center_classification_date": "20260709",
      "report_date": "20260715",
      "code_info": "Lot 0853293604  UDI-DI 03573026634551  Product is not registered in the US. OUS only."
    }
  ]
}