CareFusion 303, Inc.: Medical Device Recall in 2016 - (Recall #: Z-1179-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Alaris Pump VersaSafe Infusion Set, Model No. 2122-0007

Product Classification:

Class II

Date Initiated: February 15, 2016

Date Posted: March 23, 2016

Recall Number: Z-1179-2016

Event ID: 73238

Reason for Recall:

CareFusion is recalling the Alaris VersaSafe Infusion Set because of separation and/or leakages at the VersaSafe split septum port and tubing may lead to leakage of the administration set.

Status: Terminated

Product Quantity: 5,760 units

Code Information:

Lot No. 13085603

Distribution Pattern:

Michigan

Voluntary or Mandated:

Voluntary: Firm initiated