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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Surgical Equipment

Baxter TruSystem 7000 Operating Tables Recalled for Battery Short-Circuit

Agency Publication Date: October 24, 2024
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Summary

Baxter Healthcare Corporation is recalling approximately 8,102 TruSystem 7000 Operating Tables due to reports of battery and connector short-circuits that can emit smoke. This recall includes multiple versions of the tables, such as the U (MB), MBW, dV, V, and U14 models. The defect was discovered after reports of electrical short-circuits and smoke emission from the units during use.

Risk

A short-circuit in the battery or its connectors can cause the device to emit smoke or potentially lose power and functionality. This could disrupt surgical procedures or pose a fire and inhalation risk to patients and clinical staff in the operating room.

What You Should Do

  1. This recall affects various models of the Baxter TruSystem 7000 Operating Table, used in surgical settings for patient positioning.
  2. Identify affected units by checking the product code (REF) and Unique Device Identifier (DI) on the device label. See the Affected Products section below for the full list of affected codes.
  3. Stop using the recalled device immediately.
  4. Contact Baxter Healthcare Corporation or your medical equipment distributor to arrange for a return, replacement, or correction of the battery and connector system.
  5. Call the FDA at 1-888-463-6332 or visit www.fda.gov/medical-devices/medical-device-recalls for additional information.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: Baxter TruSystem 7000 U (MB) Operating Table
Model / REF:
1604786
1604788
1723633
Serial Numbers:
All Serial Numbers
UDI:
00887761967533
00887761967526
00887761967519

Recall #: Z-0210-2025

Product: Baxter TruSystem 7000 Operating Table
Model / REF:
1841046
Serial Numbers:
All Serial Numbers
UDI:
00887761968714

Recall #: Z-0211-2025

Product: Baxter TruSystem 7000 (MBW) Operating Table
Model / REF:
1841048
Serial Numbers:
All Serial Numbers
UDI:
00887761968714

Recall #: Z-0212-2025

Product: Baxter TruSystem 7000 (dV) Operating Table
Model / REF:
1841049
Serial Numbers:
All Serial Numbers
UDI:
00887761968691

Recall #: Z-0213-2025

Product: Baxter TruSystem 7000 V Operating Table
Model / REF:
1841050
Serial Numbers:
All Serial Numbers
UDI:
00887761974241

Recall #: Z-0214-2025

Product: Baxter TruSystem 7000 (MBW) V Operating Table
Model / REF:
1841082
Serial Numbers:
All Serial Numbers
UDI:
00887761974234

Recall #: Z-0215-2025

Product: Baxter TruSystem 7000 (dV) V Operating Table
Model / REF:
1841083
Serial Numbers:
All Serial Numbers
UDI:
00887761974227

Recall #: Z-0216-2025

Product: Baxter TruSystem 7000 U14 (MBW) Operating Table
Model / REF:
2065385
Serial Numbers:
All Serial Numbers
UDI:
00887761968653

Recall #: Z-0217-2025

Product: Baxter TruSystem 7000 U14 (MBW) V Operating Table
Model / REF:
2065386
Serial Numbers:
All Serial Numbers
UDI:
00887761973794

Recall #: Z-0218-2025

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 95409
Status: Active
Manufacturer: Baxter Healthcare Corporation
Sold By: Direct Sales; Medical Equipment Distributors
Manufactured In: United States
Units Affected: 7 products (6045 units; 397 units; 1077 units; 4 units; 24 units; 542 units; 13 units)
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.