TRUMPF MEDICAL 1704695Recalls & reported problems
Baxter Medical Systems GmbH + Co. KG · Operating table column TS7500 MOBIUS · Class 1
All models of TRUMPF MEDICAL (11)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00887761976603), received between May 24, 2023 and Jun 23, 2023 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Device Fell” (1 report).
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.
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available1
- Device Fell1
- Key or Button Unresponsive/not Working1
- No Apparent Adverse Event1
- Operating System Becomes Nonfunctional1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 23, 2023Operating System Becomes Nonfunctional; Operating System Becomes Nonfunctional
THE CUSTOMER ALLEGED THE REPORT THAT DURING A CASE WITH THE PATIENT ON THE TABLE THE COLUMN AND REMOTE AREN'T RESPONDING. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT #(B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17189362 ↗MalfunctionJun 20, 2023Appropriate Device Problem Term/Code Not Available; Device Fell; Appropriate Device Problem Term/Code Not Available; Device Fell
THE CUSTOMER ALLEGED THAT DURING THE USE OF THE TRUSYSTEM 7500 SURGICAL TABLE, AS A CAREGIVER WAS LOWERING THE TABLE, A LOUD BANG WAS HEARD, AND THE TABLE "SEEMED TO DROP." THE CUSTOMER CONFIRMED THAT NO INJURY OCCURRED WITH THIS EVENT, NO FURTHER ATTEMPTS WERE MADE TO REPOSITION THE BED, AND THE PATIENT WAS REMOVED. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17162890 ↗MalfunctionMay 24, 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 TRUSYSTEM 7500 OF THE MOBIUS AIRO CT SYSTEM IS NOT OPERATING ANYMORE. NO OPERATION WAS POSSIBLE FROM THE REMOTE CONTROL AND THE COLUMN KEYPAD. NO HARM WAS REPORTED IN RELATION TO THE ALLEGATION. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT #(B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16992315 ↗
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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