Class 2 Device Recall TruSystem 7000 U Operating Table (dV)

• Date Initiated by Firm: September 14, 2026
• Date Posted: November 03, 2026
• Recall Status: Open, Classified
• Recall Number: Z-0333-2027
• Recall Event ID: 99826
• Product Classification: Table, operating-room, electrical - Product Code GDC
• Product: Mobile column TruSystem 7500 U, Product Code 1730720
• Code Information: UDI-DI: 00887761974388; Serial number: 110183858
• FEI Number: 1416980
• Recalling Firm/ Manufacturer: Baxter Healthcare Corporation; 25212 W Il Route 120; Round Lake IL 60073-9799
• For Additional Information Contact: Center for One Baxter; 1-847-9484770
• Manufacturer Reason for Recall: 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.
• FDA Determined Cause: Equipment maintenance
• Action: Customers were notified by telephone beginning 9/14/26. Baxter Healthcare Corporation is issuing a voluntary correction for the TruSystem Surgical Tables after identifying that four units underwent spindle replacement without the required belt tension verification. The affected units were released without confirmation that belt tension met the specified requirements, which could lead to unintended downward movement of the table column. Unintended downward movement of the surgical table could occur, potentially resulting in disruption of patient positioning, reduced perfusion or oxygenation, musculoskeletal injury and/or interruption of a surgical procedure. To date, Baxter has not received any reports of patient injury related to this issue. Baxter will call to schedule a time to come in and perform the belt tension verification. Customers can continue to use the tables.
• Quantity in Commerce: 1 unit
• Distribution: US Nationwide distribution in the states of IL, MO, TX.
• Total Product Life Cycle: TPLC Device Report

¹ A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
² Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
³ The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.