Z-1419-2025 Class II Ongoing

Recalled by Baxter Healthcare Corporation — Deerfield, IL

Recall Details

Product Type
Devices
Report Date
April 2, 2025
Initiation Date
February 25, 2025
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
93 units

Product Description

Baxter TruSystem 7500 Hybrid Plus (FC), Product Code 1854087

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.

Distribution Pattern

US Nationwide distribution.

Code Information

UID/DI 00887761974067, All serial numbers manufactured until 11/14/2024.