{
  "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": "Franklin Lakes",
      "address_1": "1 Becton Dr",
      "reason_for_recall": "BD is conducting a voluntary product recall of the BD Spinal Anesthesia Tray, Cat (Ref) 405671, lot  B01K089D since a very low number of trays are incorrectly labeled as BD Single Shot Epidural Tray,  Cat (Ref) 406069.",
      "address_2": "",
      "product_quantity": "4500",
      "code_info": "B01K089D",
      "center_classification_date": "20161212",
      "distribution_pattern": "Nationwide Distribution",
      "state": "NJ",
      "product_description": "BD Spinal Anesthesia Tray  The BD Spinal Anesthesia Tray is intended for use by professional anesthesiologists to perform the spinal anesthesia procedure",
      "report_date": "20161221",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Becton Dickinson & Company",
      "recall_number": "Z-0740-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "75802",
      "termination_date": "20170912",
      "more_code_info": "",
      "recall_initiation_date": "20161107",
      "postal_code": "07417-1815",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}