{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Sparks",
      "address_1": "7 Loveton Cir",
      "reason_for_recall": "The package insert incorrectly lists the volume of the primer and probe diluent to use for the reconstitution of the master mix tube. Adding the incorrect amount of diluent could have an effect on the assay.",
      "address_2": "BD Diagnostic Systems",
      "product_quantity": "13,898",
      "code_info": "All since 08/20/2014",
      "center_classification_date": "20180428",
      "distribution_pattern": "Distributed to accounts in 8 states: CA, FL, NJ, NY, OR, PA, VA, and WI. International distribution to Argentina, Australia, Brazil, Canada, Chile, China, Colombia, Europe, Hong Kong, Japan, Singapore, Taiwan, and Thailand.",
      "state": "MD",
      "product_description": "BD MAX DNA MMK (SPC) For Laboratory Use, catalog no. 442829",
      "report_date": "20180509",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Becton Dickinson & Co.",
      "recall_number": "Z-1544-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "79769",
      "termination_date": "20180702",
      "recall_initiation_date": "20180302",
      "postal_code": "21152-9212",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}