Baxter recalls TruSystem 7500 U medical column with software issue that makes upper back unadjustable when emergency mode is enabled. Affected units have serial numbers up to 11/14/2024.
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 its TruSystem 7500 U medical column because a software problem causes the upper back section to become unadjustable when emergency mode is enabled. This could prevent proper adjustment during critical medical procedures.
The software issue causes the upper back section to become unadjustable when emergency mode is enabled. This could prevent proper adjustment of the column during critical medical procedures, potentially affecting patient care.
Healthcare facilities using the TruSystem 7500 U medical column with serial numbers up to 11/14/2024 are affected. Staff who operate the column during medical procedures are most at risk.
Check the serial number on your TruSystem 7500 U column. Affected units have serial numbers manufactured until November 14, 2024.
Verify your column's serial number to confirm if it was manufactured up to November 14, 2024.
Reach out to Baxter Healthcare Corporation for guidance on next steps.
The recall states there is a software issue that causes the upper back section to become unadjustable when emergency mode is enabled, which could affect patient care during medical procedures.
Check the serial number on your TruSystem 7500 U column. Affected units have serial numbers manufactured until November 14, 2024.
Contact Baxter Healthcare Corporation for guidance on next steps.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-1414-2025 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-1414-2025 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.
