PlainRecalls
FDA Devices Moderate Class II Ongoing

Baxter Mobile column TruSystem 7500 U, Product Code 1730720

Reported: April 2, 2025 Initiated: February 25, 2025 #Z-1413-2025

Product Description

Baxter Mobile column TruSystem 7500 U, Product Code 1730720

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.

Details

Units Affected
40 units
Distribution
US Nationwide distribution.
Location
Deerfield, IL

Frequently Asked Questions

What product was recalled?
Baxter Mobile column TruSystem 7500 U, Product Code 1730720. Recalled by Baxter Healthcare Corporation. Units affected: 40 units.
Why was this product recalled?
There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
Which agency issued this recall?
This recall was issued by the FDA Devices on April 2, 2025. Severity: Moderate. Recall number: Z-1413-2025.