Baxter recalls TruSystem 7500 medical devices with software issue preventing back section adjustment when emergency mode is enabled. Affected units have specific serial numbers and were manufactured until November 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 medical devices due to a software issue that makes the upper back section unadjustable when emergency mode is enabled. This could affect device safety during critical medical 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 compromising patient safety.
Healthcare providers using Baxter TruSystem 7500 devices with serial numbers manufactured until November 14, 2024 are most at risk. Patients receiving care through these devices may also be affected.
Check if your device has the product code 4091000 and serial numbers manufactured until November 14, 2024. The specific serial numbers are listed in the recall notice.
Verify if your TruSystem 7500 device has the product code 4091000 and serial numbers manufactured until November 14, 2024.
This recall affects Baxter TruSystem 7500 devices with product code 4091000 and serial numbers manufactured until November 14, 2024.
The recall notice does not specify a remedy, so you should check with Baxter Healthcare Corporation for further instructions.
Check the device's serial number against the list of affected units provided in the recall notice.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-1422-2025 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-1422-2025 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.
