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Use caution Medical device recall · FDA · Published September 19, 2024

Baxter TruSystem 7000 Operating Table Recall: Battery Short Circuits and Smoke Risk

Baxter Healthcare recalls TruSystem 7000 operating tables with battery short circuits and smoke emission risks. Affected units may cause fire or injury. Contact for return or repair.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-0216-2025Medical deviceBaxter Healthcare ›
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Contact the company

Recalling firmBaxter Healthcare Corporation1 Baxter Pkwy · Deerfield, IL 60015-4625
✎ GovInfoNow plain-language explainer

Baxter Healthcare is recalling its TruSystem 7000 operating tables due to reports of battery short circuits and smoke. This could lead to fire or injury if the table is used without proper maintenance. Read more at govinfonow.com/recall/53992-baxter-trusystem-7000-operating-table-recall-battery-short-circuits-and.

Source Summary by GovInfoNow · govinfonow.com/recall/53992-baxter-trusystem-7000-operating-table-recall-battery-short-circuits-and · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0216-2025

Cite this page

“Baxter TruSystem 7000 Operating Table Recall: Battery Short Circuits and Smoke Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/53992-baxter-trusystem-7000-operating-table-recall-battery-short-circuits-and. Based on FDA recall #Z-0216-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0216-2025%22&limit=1).

Baxter Healthcare Corporation voluntarily recalled its Baxter Operating Table TruSystem 7000 (dV) V due to risks of electrical short-circuits and smoke emission, according to the FDA. The Food and Drug Administration announced the Class II recall on September 19, 2024.

How to tell if you have it

  • Brand: Baxter Healthcare
  • Product: Baxter Operating Table TruSystem 7000 (dV) V
  • Product code REF 1841083
  • UDI/DI 00887761974227
  • All Serial Numbers

The hazard

The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke, according to the FDA.

Context

GovInfoNow's records show Baxter Healthcare Corporation has 187 other recalls on record since September 2, 2015. Other recent recalls of similar products include Philips Allura Xper FD10C Medical System Recall (December 15, 2025), Philips Allura Xper FD10F Medical System Recall (December 15, 2025), and Tobii Dynavox TD Navio Maxi Speech Device Recall (July 8, 2026).

How to tell if you have this one

Check for the product code REF 1841083 on the table. All units with this code are affected, including those with UDI/DI 00887761974227.

  • Brand
    Baxter Healthcare
  • Category
    Medical device
FDA recall event · 9 products

All 9 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Ongoing
  • Distribution
    Worldwide distribution.
Recall numberProduct, codes & lotsQuantity
Z-0210-2025Baxter Operating table TruSystem 7000 U (MB), Product codes: a) REF 1604786; b) REF 1604788; c) REF 1723633; a) REF 1604786, UDI/DI 00887761967533; b) REF 1604788, UDI/DI 00887761967526; c) REF 1723633, UDI/DI 00887761967519 ALL SERIAL NUMBERS6045 units
Z-0211-2025Baxter Operating Table TruSystem 7000, Product code REF 1841046; UDI/DI 00887761968714, All Serial Numbers397 units
Z-0212-2025Baxter Operating Table TruSystem 7000 (MBW), Product code REF 1841048; UDI/DI 00887761968714, All Serial NumbersN/A
Z-0213-2025Baxter Operating Table TruSystem 7000 (dV), Product code REF 1841049; UDI/DI00887761968691, All Serial Numbers1077 units
Z-0214-2025Baxter Operating Table TruSystem 7000 V, Product code REF 1841050; UDI/DI 00887761974241, All Serial Numbers4 units
Z-0215-2025Baxter Operating Table TruSystem 7000 (MBW) V, Product code REF 1841082; UDI/DI 00887761974234, All Serial Numbers24 units
Z-0216-2025Baxter Operating Table TruSystem 7000 (dV) V, Product code REF 1841083; UDI/DI 00887761974227, All Serial NumbersN/A
Z-0217-2025Baxter Operating Table TruSystem 7000 U14 (MBW), Product code REF 2065385; UDI/DI 00887761968653, All Serial Numbers542 units
Z-0218-2025Baxter Operating Table TruSystem 7000 U14 (MBW) V, Product code REF 2065386; UDI/DI 00887761973794, All Serial Numbers13 units
Based on the official FDA remedy

What to do — step by step

  1. Check for Battery Issues

    Inspect the table for signs of smoke or burning from the battery area.

  2. Contact Baxter for Details

    Reach out to Baxter Healthcare to confirm if your table is affected and get instructions.

How this recall unfolded

Recall timeline

FDA published this recall 41 days after the firm started it.

1. Firm started the recall: Sep 19, 202412. FDA classified it Class II: Oct 24, 202423. Published in FDA’s Enforcement Report: Oct 30, 202432024
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

From the GovInfoNow team · based on the FDA notice · How we make summaries

How can I tell if my table is safe to use?

If your table has no signs of smoke or burning and you've contacted Baxter, it may be safe. Otherwise, stop using it.

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Other Baxter Healthcare recalls

Baxter Healthcare Corporation recalls Welch Allyn Life2000 Compressor, Product Codes: 1) BT-80-0004; 2) BT-80-0004A; 3) BT-80-0008; 4) BT-80-0008A; 5)
April 7, 2025Baxter Healthcare Corporation recalls Welch Allyn, Inc., Life 2000 Ventilation System, REF BT-20-0002
December 20, 2024Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482; use in Peritoneal Dialysis
October 21, 2024Baxter Healthcare Corporation recalls Welch Allyn Life2000 Ventilation System, REF MS-01-0118, within exterior carton codes: 1) BT-20-0002, 2) BT-20-0002A,
September 12, 2024

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Keep exploring

Where this comes from

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.

  • Official source: FDA Recall #Z-0216-2025 (September 19, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0216-2025 to see it in context.
  • Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA