{
  "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": "Franklin Lakes",
      "address_1": "1 Becton Dr",
      "reason_for_recall": "Becton Dickinson received an elevated number of complaints for blood or infusate/medication leakage due to tearing of the silicone septum.",
      "address_2": "",
      "product_quantity": "315,800 units",
      "code_info": "Lot #'s 4128925 and 4128926",
      "center_classification_date": "20150325",
      "distribution_pattern": "Distributed to the states of CA, CT, FL, IL, MA, ND, NY, OH and PA.",
      "state": "NJ",
      "product_description": "BD Q-Syte Luer Access Split Septum, 0.16 ml, Sterile, Rx only, Catalog REF #385100, Manufacturer: Becton Dickinson Infusion Therapy Systems Inc.    An accessory to an intravascular administration set that permits injection, gravity flow or withdrawal of fluids.",
      "report_date": "20150401",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Becton Dickinson & Company",
      "recall_number": "Z-1317-2015",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "70593",
      "termination_date": "20170525",
      "more_code_info": "",
      "recall_initiation_date": "20150219",
      "postal_code": "07417-1815",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}