{
  "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": "Sparks",
      "state": "MD",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76895",
      "recalling_firm": "Bd Diagnostic",
      "address_1": "54 Loveton Circle Mc 912",
      "address_2": "N/A",
      "postal_code": "21152",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "2 US customers, 0 Ex-US regions, and 0 distributors 0.",
      "recall_number": "Z-1866-2017",
      "product_description": "BD Viper LT software, version 3.00H",
      "product_quantity": "2",
      "reason_for_recall": "BD has confirmed reports that lower than expected RFU values were generated on customer BD Viper LT Systems after the installation of software version 3.00H. As RFU values decrease, results approach the assay cutoff threshold which has the potential to impact test results.",
      "recall_initiation_date": "20151214",
      "center_classification_date": "20170419",
      "termination_date": "20170419",
      "report_date": "20170426",
      "code_info": "Catalog Number      443157  443153  443155  443156  442947  443902    Version Number                       3.00H   3.00H"
    }
  ]
}