Serious riskFDA DeviceNov 3, 2026Class II

Baxter TruSystem 7500 U mobile column recalled for lift drop risk

Baxter is recalling one TruSystem 7500 U mobile column because its main lift may unexpectedly drop from its set position to its lowest position during use. The tabletop may not be raised again after a drop, and an uncontrolled drop could cause abrupt patient displacement during surgery, which may lead to traumatic injury, airway compromise, or surgical complications.

From the FDA notice · Read the official notice ↗ · All Baxter recalls

What to do

Set the affected unit aside and do not use it for surgery.
Confirm the unit by checking serial number 110183858 and UDI-DI 00887761974388.
Contact Baxter Healthcare Corporation about the recall. The notice doesn't say how to get a repair or replacement.

Official notice ↗

Is yours affected?

Compare your label or packaging with the recalled product.

Product: Mobile column TruSystem 7500 U, Product Code 1730720
Sold in: Nationwide
Made for: All ages (0 months and older)

This recall covers 2 products — see all of them.

Details

Units affected: 1 unit
Illnesses reported: None reported
Manufactured in: 25212 W Il Route 120, Round Lake, Illinois, United States
Classification: Class II
Recall number: Z-0333-2027

In the FDA's words

Description: Mobile column TruSystem 7500 U, Product Code 1730720 The main lift may unexpectedly drop from its set position to its lowest position during use. The tabletop may not be able to be raised again after the drop occurs. An uncontrolled drop of the surgical table may result in an abrupt patient displacement during surgery. Serious or critical adverse health consequences may occur, including traumatic injury, airway compromise, and surgical procedure complications, among others. UDI-DI: 00887761974388; Serial number: 110183858 Distribution: US Nationwide distribution in the states of IL, MO, TX. Affected quantity: 1 unit
Hazard: The main lift may unexpectedly drop from its set position to its lowest position during use. The tabletop may not be able to be raised again after the drop occurs. An uncontrolled drop of the surgical table may result in an abrupt patient displacement during surgery. Serious or critical adverse health consequences may occur, including traumatic injury, airway compromise, and surgical procedure complications, among others.

2 products in this recall

Baxter TruSystem operating tables recalled for unexpected drop risk

Baxter is recalling two products: the TruSystem 7000 U Operating Table (dV), product code 1723633, and the mobile column TruSystem 7500 U, product code 1730720. The main lift may unexpectedly drop to its lowest position during use, and the tabletop may not be able to be raised again, which could cause abrupt patient displacement during surgery. The notice lists possible serious outcomes including traumatic injury and airway compromise. The products were distributed nationwide, with confirmed distribution in IL, MO and TX.

The agency lists each product separately. Check every one you might have.

TruSystem 7000 U Operating Table (dV), Product Code 1723633
Z-0332-2027 · 62 units
Mobile column TruSystem 7500 U, Product Code 1730720 (this page)
Z-0333-2027 · 1 unit