{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Hazelwood",
      "state": "MO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91617",
      "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 to the states of Alabama, California, North Carolina, and Puerto Rico.",
      "recall_number": "Z-1201-2023",
      "product_description": "MYLA comprises AST Filters in conjunction with VITEK MS; middleware which connects  microbiology laboratory instruments for ID/AST and blood culture activities and the laboratory information system (LIS).",
      "product_quantity": "19 systems",
      "reason_for_recall": "For users with MYLA V4.8.X / V4.9 that use VITEK MS to identify organisms as part of their workflow, AST filter rules that have been activated are not always being applied to AST results when sending the results to the clinician.",
      "recall_initiation_date": "20230206",
      "center_classification_date": "20230302",
      "report_date": "20230308",
      "code_info": "Versions 4.7 and 4.8",
      "more_code_info": ""
    }
  ]
}