Baxter Healthcare Corporation: Medical Device Recall in 2024 - (Recall #: Z-1001-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

Baxter Exactamix Pro 1200, REF EXM12DY

Product Classification:

Class I

Date Initiated: December 22, 2023

Date Posted: February 28, 2024

Recall Number: Z-1001-2024

Event ID: 93700

Reason for Recall:

An error was identified in software versions 2.0.8 and 2.1.8 while using the "Use Some Overfill" feature which may lead to over-delivery of an ingredient. This issue can result in redundant ingredient delivery of the requested overfill volume.

Status: Ongoing

Product Quantity: 8 devices

Code Information:

UDI/DI 05413765588150, Serial Numbers: PLD2314002, PLD2328001, PLD2328004, PLD2328042, PLD2314006, PLD2328002, PLD2328005, LD2339005

Distribution Pattern:

US: AL, AZ, CA, FL, GA, IA, KY, MD, MI, MN, MO, NC, NE, NH, NJ, NV, NY, OR, SD, TX, WA, WI,

Voluntary or Mandated:

Voluntary: Firm initiated