Baxter recalls TruSystem 7500 Hybrid (MC) with software issue where emergency mode makes upper back section unadjustable. 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 Hybrid (MC) 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 procedures.
The software issue prevents the upper back section from being adjusted when emergency mode is activated. This could lead to improper device positioning during critical medical procedures, potentially affecting patient safety.
Healthcare facilities using the Baxter TruSystem 7500 Hybrid (MC) with serial numbers up to 11/14/2024 are most at risk. Medical staff operating this device during emergencies may face safety issues.
Check for the product code 1773204 and serial numbers manufactured until November 14, 2024. The device is labeled as Baxter TruSystem 7500 Hybrid (MC).
Verify if emergency mode is enabled and whether the upper back section is adjustable.
The recall states there is a software issue that makes the upper back section unadjustable when emergency mode is enabled, which could affect patient safety during critical procedures.
Check for the product code 1773204 and serial numbers manufactured until November 14, 2024. The device is labeled as Baxter TruSystem 7500 Hybrid (MC).
The recall does not specify a remedy, so 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-1416-2025 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-1416-2025 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
