Baxter recalls TruSystem 7500 Hybrid MR IMRIS devices with software issue causing upper back section to be unadjustable in emergency mode. Affected units have specific serial numbers and were manufactured until November 2024.
There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
Baxter is recalling TruSystem 7500 Hybrid MR IMRIS devices due to a software problem that makes the upper back section unadjustable when emergency mode is enabled. This could affect device operation during critical situations.
The software issue prevents the upper back section from being adjusted when emergency mode is activated. This could lead to improper device function during critical medical procedures. The hazard is specific to emergency mode activation, not normal use.
Healthcare professionals using the TruSystem 7500 Hybrid MR IMRIS devices are most at risk. Patients receiving care through these devices may also be affected if the issue impacts treatment.
Check for the product code 2067886 on the device. Affected units have serial numbers manufactured until November 14, 2024. The full serial number is listed in the device's UID/DI section.
Verify if emergency mode is enabled and whether the upper back section is adjustable.
The device may not function properly in emergency mode, so it's recommended to check the status before use.
Look for the product code 2067886 and serial numbers manufactured until November 14, 2024.
The recall does not specify a remedy, so contact Baxter Healthcare Corporation for further guidance.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-1421-2025 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-1421-2025 from Baxter. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
