Baxter Healthcare Corporation: Medical Device Recall in 2025 - (Recall #: Z-1417-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

Baxter TruSystem 7500 Hybrid (FC), Product Code 1854085

Product Classification:

Class II

Date Initiated: February 25, 2025

Date Posted: April 2, 2025

Recall Number: Z-1417-2025

Event ID: 96286

Reason for Recall:

There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.

Status: Ongoing

Product Quantity: 10 units

Code Information:

UID/DI 00887761974081, All serial numbers manufactured until 11/14/2024.

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated