CareFusion 303, Inc.: Medical Device Recall in 2018 - (Recall #: Z-2111-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

Alaris Extension Sets with microbore tubing Model 20022 and 30914 Is used to administer fluid and medications from a syringe to the patient through a needle or catheter inserted into the patient's artery or vein. These model codes are extension sets that can be used with IV administration sets. The set s components are commonly found on intravascular administration sets and extension sets. It includes a microbore tubing, a slide clamp, male and female luer.

Product Classification:

Class II

Date Initiated: November 6, 2017

Date Posted: June 13, 2018

Recall Number: Z-2111-2018

Event ID: 80093

Reason for Recall:

Reports of incorrect priming volume due to manufacturing with incorrect tubing.

Status: Terminated

Product Quantity: 25,400 units

Code Information:

Model 20022 Lot Numbers 16087775, Model 20022 Lot Numbers 16127995 and Model 30914 Lot Numbers 16127518 and 17097167

Distribution Pattern:

US Distribution to states of: CA, IL, IN, KS, NE, NJ, TX, UT, VA and WA

Voluntary or Mandated:

Voluntary: Firm initiated