Baxter Healthcare Corporation: Medical Device Recall in 2020 - (Recall #: Z-2066-2020)

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 Control Unit

Product Classification:

Class II

Date Initiated: April 7, 2020

Date Posted: May 27, 2020

Recall Number: Z-2066-2020

Event ID: 85405

Reason for Recall:

Prismaflex product code 114870 does not have FDA regulatory clearance and was inadvertently distributed.

Status: Terminated

Product Quantity: 5 devices US territories

Code Information:

Product Code: 114870; Lot Number: PA18198, PA18199, PA18238, PA22556, PA22558.

Distribution Pattern:

Distribution only to Puerto Rico and Guam

Voluntary or Mandated:

Voluntary: Firm initiated