MAUDE Adverse Event Report: BAXTER HEALTHCARE CORPORATION HILLROM MOBILE COLUMN TRUSYSTEM 7500; TABLE, OPERATING-ROOM, ELECTRICAL

Model Number	1717023
Medical Device Problem Code	Device Fell (4014)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	09/18/2025
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Inspection of the device is pending and results will be provided by a final report.
Event or Problem Description
Baxter received a report stating that after the patient transfer to the carbon floatline tabletop, trusystem 7500 main lift of the surgical table dropped down.No harm or significant impact to the surgical procedure was reported.
Additional Manufacturer Narrative
The surgical table is intended for the following use: patient positioning during surgery, including anaesthesia induction and recovery from anaesthesia.Task-related patient transfer within the operating theatre.For applications in conjunction with intra-operative imaging (e.G.Ct, mrt, x-ray) with specific table components.The device involved in the event was inspected by a baxter field service technician.It could be confirmed that the main lift of the device could no longer be moved, and the column was in the lowest position.To correct the issue, the main lift spindle was exchanged, and the device was working as intended after this repair.The returned main lift spindle was further investigated, and wear was identified which led to a defect that could result in the allegation ¿surgical table dropped down¿.The cause was traced to a hardware defect and wear of the spindle assembly.The root cause of this wear is not established yet and will be further investigated by the supplier of this part.
Event or Problem Description
Baxter received a report stating that after the patient trasfer to the carbon floatline tabletop, trusystem 7500 main lift of the surgical table dropped down.No harm or significant impact to the surgical procedure was reported.

• Brand Name: HILLROM MOBILE COLUMN TRUSYSTEM 7500
• Common Device Name: TABLE, OPERATING-ROOM, ELECTRICAL
• Manufacturer (Section D): BAXTER HEALTHCARE CORPORATION; deerfield IL
• Manufacturer (Section G): BAXTER MEDICAL SYSTEMS GMBH + CO. KG; carl zeiss strasse 7-9; null; saalfeld thuringen 07318 ; GM 07318
• Manufacturer Contact: 25212 w. illinois route 120; round lake, IL 60073 ; 2242702068
• MDR Report Key: 23168637
• Report Number: 3007143268-2025-00071
• Device Sequence Number: 9639544
• Product Code: GDC
• UDI-Device Identifier: 00887761993150
• UDI-Public: (01)00887761993150(11)240814
• Combination Product (Y/N): N
• Initial Reporter Country: GM
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Foreign,Health Professional,Company Representative
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 11/26/2025

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Model Number: 1717023
• Device Catalogue Number: 1717023
• Device Lot Number: N/A
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 09/18/2025
• Supplement Date Received by Manufacturer: 11/14/2025
• Initial Report FDA Received Date: 09/29/2025
• Supplement Report FDA Received Date: 11/26/2025
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 08/14/2024
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Reuse
• Patient Sequence Number: 1
• Patient Sex: Unknown