Baxter recalls TruSystem 7000 operating tables with battery short circuits and smoke emission risks. Affected units have specific product codes and serial numbers. Contact Baxter for details.
The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.
Baxter is recalling its TruSystem 7000 operating tables due to reports of battery short circuits and smoke. This could lead to electrical hazards if the table is used improperly.
The batteries and connectors in these operating tables can short circuit and emit smoke, which may cause electrical hazards. This risk is particularly concerning in medical settings where equipment is used frequently.
Healthcare facilities using Baxter TruSystem 7000 operating tables with the specified product code and serial numbers are most at risk. Patients and staff could be affected if the table malfunctions.
Check for the product code REF 1841048 and serial numbers on the table. The recall includes all units with UDI/DI 00887761968714.
Verify the product code REF 1841048 and serial numbers on your Baxter TruSystem 7000 operating table.
Baxter received customer reports that the batteries and connectors experienced electrical short-circuits and/or emitted smoke.
Check the product code and serial numbers to see if your table is affected. Contact Baxter for further instructions.
The recall record does not specify a remedy or fix.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-0212-2025 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-0212-2025 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.