{
  "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 III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70645",
      "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": "Worldwide Distribution to United Kingdom and Turkey.  NO U.S. distribution.",
      "recall_number": "Z-1403-2015",
      "product_description": "Vitek 2 AST-P641 REF 418 590 Gram Positive 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 Staphylococcus spp., Enterococcus spp., and S. agalactiae.",
      "product_quantity": "1505 cartons",
      "reason_for_recall": "The outer carton label and package insert for the recalled product incorrectly lists Streptococcus pneumoniae as an organism for intended use.",
      "recall_initiation_date": "20150225",
      "center_classification_date": "20150408",
      "termination_date": "20170322",
      "report_date": "20150415",
      "code_info": "lot 741350820, expiration 22JUL16;  lot 741340920, expiration 14APR16;"
    }
  ]
}