Baxter recalls TruSystem 7500 Hybrid (FC) units with software issue causing emergency mode to be unresponsive. Affected units have product code 1854085 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 TruSystem 7500 Hybrid (FC) medical devices due to a software issue that makes the emergency mode unresponsive. This could prevent proper adjustment of the upper back section when emergency mode is activated, potentially affecting patient safety during critical situations.
The software issue causes the upper back section to become unresponsive when emergency mode is enabled. This could prevent critical adjustments needed during emergencies, potentially compromising patient safety if the device fails to function properly under stress.
Healthcare facilities using Baxter TruSystem 7500 Hybrid (FC) devices with product code 1854085 and serial numbers manufactured through November 14, 2024 are affected. Medical staff who rely on these devices for patient care are most at risk.
Check for product code 1854085 on the device label. Affected units have serial numbers manufactured up to November 14, 2024. The device model is Baxter TruSystem 7500 Hybrid (FC).
Verify if emergency mode is responsive by attempting to adjust the upper back section.
This recall applies to Baxter TruSystem 7500 Hybrid (FC) devices with product code 1854085 and serial numbers manufactured through November 14, 2024.
The recall does not specify a remedy, so contact Baxter Healthcare Corporation directly for guidance.
Check for product code 1854085 on the device label and serial numbers manufactured up to November 14, 2024.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-1417-2025 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-1417-2025 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.
