{
  "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": [
    {
      "status": "Terminated",
      "city": "Sparks",
      "state": "MD",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "78102",
      "recalling_firm": "Becton Dickinson & Co.",
      "address_1": "7 Loveton Cir",
      "address_2": "N/A",
      "postal_code": "21152-9212",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US including CA, NC & TN  Internationally: Canada",
      "recall_number": "Z-0198-2018",
      "product_description": "BD PhoenixTM AP, Catalog Number 448010  The BD Phoenix\" AP instrument is designed for use with the BD Phoenix\" system is intended to standardize ID broth tube inoculum, add AST indicator to the AST broth tube and transfer an aliquot of ID broth to AST broth tubes, as required for preparing samples for use on the BD Phoenix\" system, which performs identification and susceptibility testing",
      "product_quantity": "7 units",
      "reason_for_recall": "Potential unexpected movement of robot arm",
      "recall_initiation_date": "20170601",
      "center_classification_date": "20171206",
      "termination_date": "20180509",
      "report_date": "20171213",
      "code_info": "Serial Numbers: AP0447, AP0448, AP0449, AP0450, AP0451, AP0458 & AP0463.",
      "more_code_info": ""
    }
  ]
}