Baxter Healthcare Corporation: Medical Device Recall in 2018 - (Recall #: Z-0485-2018)

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:

Empty IntraVia Container with Non-DEHP Fluid Path, 500mL Containers are intended for use in the preparation and administration of drug admixtures.

Product Classification:

Class II

Date Initiated: July 27, 2017

Date Posted: February 7, 2018

Recall Number: Z-0485-2018

Event ID: 78042

Reason for Recall:

A leak may allow for microbial contamination of the sterile fluid path.

Status: Terminated

Product Quantity: 29,088 units

Code Information:

Product Code 2J8003, Lot No. DR16J18096.

Distribution Pattern:

Distribution in the US and Canada.

Voluntary or Mandated:

Voluntary: Firm initiated