TRUMPF MEDICAL 1717020Recalls & reported problems
Baxter Medical Systems GmbH + Co. KG · Hillrom™ Stationary column TruSystem 7500 · Class 1
All models of TRUMPF MEDICAL (11)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00887761985865), received between Oct 26, 2022 and Aug 19, 2025 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Key or Button Unresponsive/not Working” (2 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Key or Button Unresponsive/not Working2
- Device Fell1
- No Apparent Adverse Event1
- Unintended Movement1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 19, 2025Key or Button Unresponsive/not Working; Key or Button Unresponsive/not Working
BAXTER RECEIVED A REPORT STATING THAT STATIONARY COLUMN TRUSYSTEM 7500 WAS HAVING A TOTAL LOSS OF FUNCTION. NO HARM OR SIGNIFICANT IMPACT TO THE SURGICAL PROCEDURE WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22841843 ↗MalfunctionJul 25, 2025Unintended Movement; Unintended Movement
BAXTER RECEIVED A REPORT STATING THAT DURING A PROCEDURE, STATIONARY COLUMN TRUSYSTEM 7500 WAS ADJUSTED SLIGHTLY TO TRENDELENBURG, BUT SHORTLY THEREAFTER, THE TABLE AUTOMATICALLY ADJUSTED TO FULL TRENDELENBURG. THE SURGICAL TEAM MANAGED TO PREVENT THE PATIENT FROM SLIDING OFF. NO HARM OR SIGNIFICANT IMPACT TO THE SURGICAL PROCEDURE WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22611000 ↗MalfunctionFeb 16, 2023No Apparent Adverse Event; Key or Button Unresponsive/not Working; No Apparent Adverse Event; Key or Button Unresponsive/not Working
THE CUSTOMER ALLEGED THAT THE OPERATING TABLE FROZE WHILE ANESTHETIZING THE PATIENT AND GIVES POWER SUPPLY ERROR. NO HARM OR INJURY TO PATIENT OR CAREGIVER WAS REPORTED. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT # (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16384676 ↗MalfunctionOct 26, 2022Device Fell; Device Fell
THE CUSTOMER ALLEGED THAT THE OPERATING TABLE COLUMN DROPPED DOWN WITH THE PATIENT ON THE TABLE TOP. THIS OCCURRED AFTER THE SURGICAL PROCEDURE WHEN THE PATIENT SHOULD BE REMOVED FROM THE OR. THE HEIGHT ADJUSTMENT OF THE COLUMN DOESN'T WORK ANYMORE. NO HARM OR INJURY TO PATIENT OR CAREGIVER WAS REPORTED. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT # (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15673067 ↗
Other TABLE, SURGICAL WITH ORTHOPEDIC ACCESSORIES, AC-POWERED devices
- TS 7000 1604788Baxter Medical Systems GmbH + Co. KG · TABLE, SURGICAL WITH ORTHOPEDIC ACCESSORIES, AC-POWERED1 recall4 reports
- TS 7500 1717023Baxter Medical Systems GmbH + Co. KG · TABLE, SURGICAL WITH ORTHOPEDIC ACCESSORIES, AC-POWERED1 recall1 report
- TS 7500 1704695Baxter Medical Systems GmbH + Co. KG · TABLE, SURGICAL WITH ORTHOPEDIC ACCESSORIES, AC-POWERED1 recall0 reports
- TS 7500 1854085Baxter Medical Systems GmbH + Co. KG · TABLE, SURGICAL WITH ORTHOPEDIC ACCESSORIES, AC-POWERED1 recall0 reports
- TS 7500 1854087Baxter Medical Systems GmbH + Co. KG · TABLE, SURGICAL WITH ORTHOPEDIC ACCESSORIES, AC-POWERED1 recall0 reports
- ADVANCED CONTROL I-BASE, DC 5803Mizuho Orthopedic Systems, Inc. · Table, Surgical With Orthopedic Accessories, Ac-Powered47 reports
- TRUMPF MEDICAL 1723633Baxter Medical Systems GmbH + Co. KG · TABLE, SURGICAL WITH ORTHOPEDIC ACCESSORIES, AC-POWERED43 reports
- TABLE, HANA, 110 V 6875Mizuho Orthopedic Systems, Inc. · Table, Surgical With Orthopedic Accessories, Ac-Powered2 deaths36 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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