Baxter recalls TruSystem 7500 Hybrid Plus (FC) with software issue where emergency mode makes upper back section unadjustable. Affected units have product code 1854087 and 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 Hybrid Plus (FC) medical device due to a software issue that makes the upper back section unadjustable when emergency mode is enabled. This could affect patient safety during critical medical procedures.
The software issue causes the upper back section to become unadjustable when emergency mode is activated. This could prevent proper adjustment of critical medical equipment during emergencies, potentially affecting patient safety.
Healthcare facilities using the Baxter TruSystem 7500 Hybrid Plus (FC) device with product code 1854087 are most at risk. Patients receiving care through this equipment could be impacted if the issue occurs during emergency procedures.
Check for product code 1854087 on the device. Affected units have serial numbers manufactured until November 14, 2024. The device is labeled as "Baxter TruSystem 7500 Hybrid Plus (FC)."
Verify if emergency mode activation makes the upper back section unadjustable.
The recall indicates a software issue that could make the upper back section unadjustable when emergency mode is enabled, so it should not be used until the issue is resolved.
Check for product code 1854087 and serial numbers manufactured until November 14, 2024.
The recall does not specify a remedy, so contact Baxter Healthcare Corporation for guidance.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-1419-2025 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-1419-2025 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.
