CareFusion 303, Inc.: Medical Device Recall in 2014 - (Recall #: Z-1459-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

SmartSite Extension Set, Model No. 20029E, intravascular administration set.

Product Classification:

Class II

Date Initiated: March 19, 2014

Date Posted: April 23, 2014

Recall Number: Z-1459-2014

Event ID: 67774

Reason for Recall:

Disconnections and leakages at the connection of the smallbore tubing and the SmartSite Y-port.

Status: Terminated

Product Quantity: 7,700 units

Code Information:

Lot No. 13085791

Distribution Pattern:

USA Nationwide Distribution in the states of: AR, AZ, CA, CO, FL, ID, MD, MI, NC, NV, OK, OR, PA, TX, VA, WI

Voluntary or Mandated:

Voluntary: Firm initiated