{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Hazelwood",
      "state": "MO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70868",
      "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": "Distributed only to foreign subsidiaries and distributors, including Canada and Mexico.",
      "recall_number": "Z-1603-2015",
      "product_description": "Vitek 2 AST-YS01 REF 22 108, Fungal Susceptibility Card, 20 cards per carton, IVD.      Intended for use with the Vitek 2 Systems in clinical laboratories as an in vitro test to determine the susceptibility of clinically significant yeasts to antifungal agents when used as instructed.",
      "product_quantity": "1604/20-card cartons",
      "reason_for_recall": "The test kits have Out-of-Range-Low (OORL) Flucytosine QC results for Candida krusei ATCC 6258.",
      "recall_initiation_date": "20150327",
      "center_classification_date": "20150512",
      "termination_date": "20170324",
      "report_date": "20150520",
      "code_info": "lot 281317710, 26-AUG-15;  lot 281347810, 22-JUN-16; and lot 281350120, 15-JUL-16.",
      "more_code_info": ""
    }
  ]
}