Baxter TruSystem 7500 Operating Tables Recalled for Software Control Failure

Agency Publication Date: March 21, 2025

Summary

Baxter Healthcare Corporation is recalling 4,542 units of TruSystem 7500 operating tables because of a software defect. This issue causes the upper back section of the table to become inoperable or impossible to adjust when the "emergency mode" function is turned on. The recall affects various configurations, including mobile, stationary, and floor-mounted models manufactured until November 14, 2024. No injuries have been reported to date.

Risk

If the upper back section of the operating table cannot be adjusted during a medical procedure while in emergency mode, healthcare providers may be unable to properly position the patient. This could lead to surgical complications, delays in critical treatment, or patient injury during an emergency situation.

What You Should Do

This recall involves several configurations of the Baxter TruSystem 7500 Operating Table, including Mobius, Stationary, Floor mounting, Mobile, and Hybrid models manufactured through November 14, 2024.
Check your operating table for the product codes and Unique Device Identifier (UDI) numbers listed on the device identification label. Affected product codes include 1704695, 1717020, 1717021, 1717023, 1730720, 1730731, 1730732, 1773204, 1854085, 1854086, 1854087, 1854088, 2067886, and 4091000. See the Affected Products section below for the full list of affected codes.
Stop using the recalled device. Contact Baxter Healthcare Corporation or your authorized medical device distributor to arrange for a return, replacement, or software correction.
Call the FDA at 1-888-463-6332 (1-888-INFO-FDA) or visit www.fda.gov/medical-devices/medical-device-recalls for additional information regarding this recall.

Your Remedy Options

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 Operating table column TS7500 MOBIUS

Model / REF:

1704695

Serial Numbers:

All serial numbers manufactured until 11/14/2024

UDI:

00887761974425

Recall #: Z-1409-2025; Quantity: 403 units

Product: Baxter Stationary column TruSystem 7500

Model / REF:

1717020

Serial Numbers:

All serial numbers manufactured until 11/14/2024

UDI:

00887761974418

Recall #: Z-1410-2025; Quantity: 462 units

Product: Baxter Floor mounting column TruSystem 7500

Model / REF:

1717021

Serial Numbers:

All serial numbers manufactured until 11/14/2024

UDI:

00887761974401

Recall #: Z-1411-2025; Quantity: 112 units

Product: Baxter Mobile column TruSystem 7500

Model / REF:

1717023

Serial Numbers:

All serial numbers manufactured until 11/14/2024

UDI:

00887761974395

Recall #: Z-1412-2025; Quantity: 1596 units

Product: Baxter Mobile column TruSystem 7500 U

Model / REF:

1730720

Serial Numbers:

All serial numbers manufactured until 11/14/2024

UDI:

00887761974388

Recall #: Z-1413-2025; Quantity: 40 units

Product: Baxter Stationary column TruSystem 7500 U

Model / REF:

1730731

Serial Numbers:

All serial numbers manufactured until 11/14/2024

UDI:

00887761974371

Recall #: Z-1414-2025; Quantity: 2 units

Product: Baxter Floor mounting column TS 7500 U

Model / REF:

1730732

Serial Numbers:

All serial numbers manufactured until 11/14/2024

UDI:

00887761974364

Recall #: Z-1415-2025; Quantity: 33 units

Product: Baxter TruSystem 7500 Hybrid (MC)

Model / REF:

1773204

Serial Numbers:

All serial numbers manufactured until 11/14/2024

UDI:

00887761974326

Recall #: Z-1416-2025; Quantity: 2 units

Product: Baxter TruSystem 7500 Hybrid (FC)

Model / REF:

1854085

Serial Numbers:

All serial numbers manufactured until 11/14/2024

UDI:

00887761974081

Recall #: Z-1417-2025; Quantity: 10 units

Product: Baxter TruSystem 7500 Hybrid (SC)

Model / REF:

1854086

Serial Numbers:

All serial numbers manufactured until 11/14/2024

UDI:

00887761974074

Recall #: Z-1418-2025; Quantity: 8 units

Product: Baxter TruSystem 7500 Hybrid Plus (FC)

Model / REF:

1854087

Serial Numbers:

All serial numbers manufactured until 11/14/2024

UDI:

00887761974067

Recall #: Z-1419-2025; Quantity: 93 units

Product: Baxter TruSystem 7500 Hybrid Plus (SC)

Model / REF:

1854088

Serial Numbers:

All serial numbers manufactured until 11/14/2024

UDI:

00887761974050

Recall #: Z-1420-2025; Quantity: 48 units

Product: Baxter TruSystem 7500 Hybrid MR IMRIS

Model / REF:

2067886

Serial Numbers:

All serial numbers manufactured until 11/14/2024

UDI:

00887761973763

Recall #: Z-1421-2025; Quantity: 24 units

Product: Baxter TruSystem 7500

Model / REF:

4091000

Serial Numbers:

All serial numbers manufactured until 11/14/2024

UDI:

00887761968639

Recall #: Z-1422-2025; Quantity: 1709 units

Additional Information

Agency: Food and Drug Administration (FDA)

Event ID: 96286

Status: Active

Manufacturer: Baxter Healthcare Corporation

Sold By: Baxter Healthcare Corporation; Authorized Medical Device Distributors

Manufactured In: United States

Units Affected: 14 products (403 units; 462 units; 112 units; 1596 units; 40 units; 2 units; 33 units; 2 units; 10 units; 8 units; 93 units; 48 units; 24 units; 1709 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 · 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.

Summary

Risk

What You Should Do

This recall involves several configurations of the Baxter TruSystem 7500 Operating Table, including Mobius, Stationary, Floor mounting, Mobile, and Hybrid models manufactured through November 14, 2024.

Check your operating table for the product codes and Unique Device Identifier (UDI) numbers listed on the device identification label. Affected product codes include 1704695, 1717020, 1717021, 1717023, 1730720, 1730731, 1730732, 1773204, 1854085, 1854086, 1854087, 1854088, 2067886, and 4091000. See the Affected Products section below for the full list of affected codes.

Stop using the recalled device. Contact Baxter Healthcare Corporation or your authorized medical device distributor to arrange for a return, replacement, or software correction.

Call the FDA at 1-888-463-6332 (1-888-INFO-FDA) or visit www.fda.gov/medical-devices/medical-device-recalls for additional information regarding this recall.

Affected Products

Product: Baxter Operating table column TS7500 MOBIUS

Model / REF:

1704695

Serial Numbers:

All serial numbers manufactured until 11/14/2024

UDI:

00887761974425

Recall #: Z-1409-2025; Quantity: 403 units

Product: Baxter Stationary column TruSystem 7500

Model / REF:

1717020

Serial Numbers:

All serial numbers manufactured until 11/14/2024

UDI:

00887761974418

Recall #: Z-1410-2025; Quantity: 462 units

Product: Baxter Floor mounting column TruSystem 7500

Model / REF:

1717021

Serial Numbers:

All serial numbers manufactured until 11/14/2024

UDI:

00887761974401

Recall #: Z-1411-2025; Quantity: 112 units

Product: Baxter Mobile column TruSystem 7500

Model / REF:

1717023

Serial Numbers:

All serial numbers manufactured until 11/14/2024

UDI:

00887761974395

Recall #: Z-1412-2025; Quantity: 1596 units

Product: Baxter Mobile column TruSystem 7500 U

Model / REF:

1730720

Serial Numbers:

All serial numbers manufactured until 11/14/2024

UDI:

00887761974388

Recall #: Z-1413-2025; Quantity: 40 units

Product: Baxter Stationary column TruSystem 7500 U

Model / REF:

1730731

Serial Numbers:

All serial numbers manufactured until 11/14/2024

UDI:

00887761974371

Recall #: Z-1414-2025; Quantity: 2 units

Product: Baxter Floor mounting column TS 7500 U

Model / REF:

1730732

Serial Numbers:

All serial numbers manufactured until 11/14/2024

UDI:

00887761974364

Recall #: Z-1415-2025; Quantity: 33 units

Product: Baxter TruSystem 7500 Hybrid (MC)

Model / REF:

1773204

Serial Numbers:

All serial numbers manufactured until 11/14/2024

UDI:

00887761974326

Recall #: Z-1416-2025; Quantity: 2 units

Product: Baxter TruSystem 7500 Hybrid (FC)

Model / REF:

1854085

Serial Numbers:

All serial numbers manufactured until 11/14/2024

UDI:

00887761974081

Recall #: Z-1417-2025; Quantity: 10 units

Product: Baxter TruSystem 7500 Hybrid (SC)

Model / REF:

1854086

Serial Numbers:

All serial numbers manufactured until 11/14/2024

UDI:

00887761974074

Recall #: Z-1418-2025; Quantity: 8 units

Product: Baxter TruSystem 7500 Hybrid Plus (FC)

Model / REF:

1854087

Serial Numbers:

All serial numbers manufactured until 11/14/2024

UDI:

00887761974067

Recall #: Z-1419-2025; Quantity: 93 units

Product: Baxter TruSystem 7500 Hybrid Plus (SC)

Model / REF:

1854088

Serial Numbers:

All serial numbers manufactured until 11/14/2024

UDI:

00887761974050

Recall #: Z-1420-2025; Quantity: 48 units

Product: Baxter TruSystem 7500 Hybrid MR IMRIS

Model / REF:

2067886

Serial Numbers:

All serial numbers manufactured until 11/14/2024

UDI:

00887761973763

Recall #: Z-1421-2025; Quantity: 24 units

Product: Baxter TruSystem 7500

Model / REF:

4091000

Serial Numbers:

All serial numbers manufactured until 11/14/2024

UDI:

00887761968639

Recall #: Z-1422-2025; Quantity: 1709 units

Additional Information

Agency: Food and Drug Administration (FDA)

Event ID: 96286

Status: Active

Manufacturer: Baxter Healthcare Corporation

Sold By: Baxter Healthcare Corporation; Authorized Medical Device Distributors

Manufactured In: United States

Units Affected: 14 products (403 units; 462 units; 112 units; 1596 units; 40 units; 2 units; 33 units; 2 units; 10 units; 8 units; 93 units; 48 units; 24 units; 1709 units)

Distributed To: Nationwide