Baxter Healthcare Corporation: Medical Device Recall in 2020 - (Recall #: Z-1831-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Prismaflex System, Prismaflex Control Unit

Product Classification:

Class II

Date Initiated: February 6, 2020

Date Posted: May 6, 2020

Recall Number: Z-1831-2020

Event ID: 85007

Reason for Recall:

Baxter is communicating safety information from the Prismaflex Operator's Manual regarding the proper use of connectors with the Prismaflex system.

Status: Terminated

Product Quantity: 555

Code Information:

Product Code:115269; GTIN 07332414117702

Distribution Pattern:

Distribution in US, Puerto Rico

Voluntary or Mandated:

Voluntary: Firm initiated