{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Sparks",
      "address_1": "BD Diagnostic Systems",
      "reason_for_recall": "Electrical power module installed on some in vitro diagnostic instruments does not meet industry standards as labeled.",
      "address_2": "7 Loveton Circle",
      "product_quantity": "71 instruments",
      "code_info": "Serial Numbers: CT0173 to CT0249, CT0253 to CT0260, CT0262, CT0263, CT0265, CT0269, and CT0272",
      "center_classification_date": "20130703",
      "distribution_pattern": "Worldwide Distribution - USA Nationwide and in the countries of:  Japan, Singapore, Hong Kong, China, Australia, Europe, and Chile.",
      "state": "MD",
      "product_description": "BD MAX Instrument, catalog #441916     Product Usage:  The BD MAX System, used in conjunction with the appropriate extraction kits and reagents is capable of automated amplification and detection of target nucleic acid sequences for use in clinical, industrial, and research settings.",
      "report_date": "20130710",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Becton Dickinson & Co.",
      "recall_number": "Z-1662-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "65431",
      "termination_date": "20130819",
      "recall_initiation_date": "20130531",
      "postal_code": "21152-0999",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}