Baxter Healthcare recalls TruSystem 7000 V operating tables with electrical short-circuits and smoke emissions. Affected units have specific product codes and serial numbers.
The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.
Baxter Healthcare is recalling its TruSystem 7000 V operating tables due to reports of batteries causing electrical short-circuits and smoke. This could lead to fire or injury if the table is used improperly.
Batteries in the operating table can short-circuit and emit smoke, which may cause fire or injury. This hazard occurs when the table is in use, especially during electrical stress.
Healthcare facilities using Baxter TruSystem 7000 V operating tables are most at risk. Patients and staff could be affected if the table malfunctions during surgery.
Check for product code REF 1841050 or serial numbers starting with 00887761974241. The table is sold under the name 'Baxter Operating Table TruSystem 7000 V'.
Identify the product code REF 1841050 or serial numbers starting with 00887761974241.
Baxter Healthcare received customer reports that the batteries and connectors experienced electrical short-circuits and/or emitted smoke.
Check for product code REF 1841050 or serial numbers starting with 00887761974241.
The recall record does not specify a remedy, so contact Baxter Healthcare directly for guidance.
We’ve drafted a message you can send Baxter Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0214-2025 — Baxter Healthcare Baxter Healthcare Hello, I own a Baxter Healthcare that is covered by recall Z-0214-2025 from Baxter Healthcare. 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.