Becton Dickinson & Company: Medical Device Recall in 2015 - (Recall #: Z-1317-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

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.

Product Classification:

Class II

Date Initiated: February 19, 2015

Date Posted: April 1, 2015

Recall Number: Z-1317-2015

Event ID: 70593

Reason for Recall:

Becton Dickinson received an elevated number of complaints for blood or infusate/medication leakage due to tearing of the silicone septum.

Status: Terminated

Product Quantity: 315,800 units

Code Information:

Lot #'s 4128925 and 4128926

Distribution Pattern:

Distributed to the states of CA, CT, FL, IL, MA, ND, NY, OH and PA.

Voluntary or Mandated:

Voluntary: Firm initiated