TRUMPF MEDICALRecalls & reported problems across all models
Baxter Medical Systems GmbH + Co. KG · 11 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 78
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls
- 0
We found 11 models of TRUMPF MEDICAL by Baxter Medical Systems GmbH + Co. KG in the FDA's device registry (GUDID). Together they are named in 78 adverse event reports in the FDA's MAUDE database, received between Jan 13, 2021 and Aug 14, 2026 — classified as 2 injuries, 76 malfunctions.
The most frequently reported specific device problem is “Unintended Movement” (30 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported TRUMPF MEDICAL problems
Device problems
- Unintended Movement30
- Operating System Becomes Nonfunctional13
- Key or Button Unresponsive/not Working10
- No Apparent Adverse Event7
- Device Fell6
- Unstable5
- Appropriate Device Problem Term/Code Not Available3
- Mechanical Problem3
Patient problems
- No Clinical Signs, Symptoms or Conditions75
- Liver Laceration(s)2
- No Consequences Or Impact To Patient1
- No Patient Involvement1
TRUMPF MEDICAL models
11 models, most reported first. Each model has its own page with its reports, recalls and device details.
- TRUMPF MEDICAL 1723633TABLE, SURGICAL WITH ORTHOPEDIC ACCESSORIES, AC-POWERED43 reports
- TRUMPF MEDICAL 1604788TABLE, OPERATING-ROOM, ELECTRICAL11 reports
- Trumpf Medical 4080100Table, radiologic9 reports
- TRUMPF MEDICAL 1717020TABLE, SURGICAL WITH ORTHOPEDIC ACCESSORIES, AC-POWERED4 reports
- TRUMPF MEDICAL 1704695TABLE, SURGICAL WITH ORTHOPEDIC ACCESSORIES, AC-POWERED3 reports
- TRUMPF MEDICAL 4091000Table, radiologic3 reports
- TRUMPF MEDICAL 1853828Table, radiologic1 report
- TRUMPF MEDICAL 1489491TABLE, SURGICAL WITH ORTHOPEDIC ACCESSORIES, AC-POWERED1 report
- TRUMPF MEDICAL 1730732TABLE, SURGICAL WITH ORTHOPEDIC ACCESSORIES, AC-POWERED1 report
- TRUMPF MEDICAL 1717023Table, radiologic1 report
- Trumpf Medical 4038120Lamp, operating-room1 report
Recent TRUMPF MEDICAL adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionAug 14, 2026Unintended Movement
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50261249 ↗MalfunctionAug 11, 2026Unstable
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50212129 ↗MalfunctionApr 21, 2026Unstable
DURING COMPLAINT EVALUATION WAS FOUND THAT TABLE PST 500 HAD WOBBLING MOVEMENT WHEN THE TABLETOP WAS PUSHED. THIS OCCURRED DURING PATIENT USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24940021 ↗MalfunctionMar 23, 2026Unintended Movement
ON (B)(6) 2026, A COMPANY REPRESENTATIVE/SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT OPERATING TABLE TRUSYSTEM 7000 (PRODUCT CODE 1723633, SERIAL NUMBER (B)(6)), THE TABLE IS GOING UP AND DOWN ON ITS OWN. THIS OCCURRED DURING PATIENT USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24667249 ↗MalfunctionDec 26, 2025Unintended Movement; Device Fell; Unintended Movement; Device Fell
BAXTER RECEIVED A REPORT STATING THAT DURING A SURGICAL PROCEDURE, A OPERATING TABLE TRUSYSTEM 7000 HAD LIFTED ONE FOOT OFF THE GROUND AT ONE END OF THE TABLE. THE CUSTOMER THEN REVERSED THE POSITION AND THE TABLE LOWERED RAPIDLY. THIS OCCURRED DURING PATIENT USE. THE PATIENT WAS UNINJURED, AND THE PROCEDURE WAS FINISHED WITHOUT INCIDENT. NO HARM OR SIGNIFICANT IMPACT TO THE SURGICAL PROCEDURE WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23898920 ↗MalfunctionDec 22, 2025Unintended Movement; Unintended Movement
ON 25-NOV-2025, A OTHER HEALTH CARE PROFESSIONAL CONTACTED TECHNICAL SERVICE TO REPORT THAT PST 500 (PRODUCT CODE 4080100, SERIAL NUMBER (B)(6)), HAD AN ISSUE, THE BRAKES DO NOT EXTEND EVENLY, CAUSING THE OPERATING TABLE TO WOBBLE. ONE BRAKE RELEASES INTRAOPERATIVELY, CAUSING THE OPERATING TABLE TO WOBBLE. THIS OCCURRED DURING PATIENT USE. THERE WAS NO PATIENT INJURY OR DEATH REPORTED WITH THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23872421 ↗MalfunctionNov 21, 2025Unintended Movement; Unintended Movement
ANOTHER HEALTH CARE PROFESSIONAL CONTACTED TECHNICAL SERVICE TO REPORT THAT THE PST 500 HAD AN ISSUE, THE HYDRAULIC STAMPS WERE DISENGAGING ON ITS OWN. NO HARM OR SIGNIFICANT IMPACT TO THE SURGICAL PROCEDURE WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23619417 ↗MalfunctionNov 18, 2025Key or Button Unresponsive/not Working; Key or Button Unresponsive/not Working
IT WAS REPORTED THAT OR TABLE TRUSYSTEM 7000 U (PRODUCT CODE 1604788, SERIAL NUMBER (B)(6)), SURGICAL TABLE LOST ALL POWER AND FUNCTION. THERE WAS NO REPORT OF PATIENT INJURY HOWEVER, THERE WAS A REPORTED ¿LONG DELAY¿ IN THE PROCEDURE DUE TO THE INABILITY TO UNLOCK THE TABLE AND MOVE IT OUT OF THE ROOM. FOLLOW UP WITH THE CUSTOMER FOUND THAT THE STAFF ATTEMPTED TO REPOSITION THE TABLE PRIOR TO THE INCISION. THE STAFF ATTEMPTED TO TROUBLESHOOT, USING THE REMOTE AND RESETTING THE BED BY POWERING OFF AND BACK ON. IT WAS REPORTED THAT FOUR OF THE STAFF LIFTED THE BED AND MOVED THE TABLE TO THE SIDE SO THE PROCEDURE COULD CONTINUE. IT WAS REPORTED BY THE CUSTOMER THAT THE DELAY WAS ESTIMATED TO BE ABOUT 30 MINUTES. NO PATIENT INJURY WAS REPORTED, AND THE PATIENT WAS TRANSFERRED TO A DIFFERENT TABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23586249 ↗MalfunctionNov 12, 2025Key or Button Unresponsive/not Working; Key or Button Unresponsive/not Working
BAXTER RECEIVED A REPORT STATING THAT OR TABLE TRUSYSTEM 7000 U WAS NOT MOVING WITH ANY FUNCTIONS WITH KEYPAD OR REMOTE. NO HARM OR SIGNIFICANT IMPACT TO THE SURGICAL PROCEDURE WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23539343 ↗MalfunctionNov 10, 2025Unintended Movement; Unintended Movement
BAXTER RECEIVED A REPORT STATING THAT OR TABLE TRUSYSTEM 7000 U HEAD SECTION WILL NOT STAY IN PLACE. NO HARM OR SIGNIFICANT IMPACT TO THE SURGICAL PROCEDURE WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23511856 ↗MalfunctionSep 29, 2025Device Fell; Device Fell
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.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23168637 ↗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 ↗MalfunctionJun 25, 2025Device Fell; Device Fell
BAXTER RECEIVED A REPORT STATING THAT OR TABLE TRUSYSTEM 7000 U (DV) EAD SECTION FELL OFF OF THE TABLE DURING A SURGICAL PROCEDURE WITH A PATIENT ON THE TABLE. THE BED WAS LOCATED AT THE ACCOUNT AND NO HARM OR SIGNIFICANT IMPACT TO THE SURGICAL PROCEDURE WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22330871 ↗MalfunctionJun 24, 2025Unintended Movement; Unintended Movement
BAXTER RECEIVED A REPORT STATING THAT CUSTOMER WAS TRYING TO LOWER THE TABLE TRUSYSTEM 7000 U (DV) AND IT WAS NOT FUNCTIONAL. SUDDENLY, THE TABLE DROPPED 5-6". THE BED WAS LOCATED AT THE ACCOUNT AND OCCURRED DURING A CASE. NO HARM OR SIGNIFICANT IMPACT TO THE SURGICAL PROCEDURE WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22318255 ↗
Other Baxter Medical Systems GmbH + Co. KG products
All Baxter Medical Systems GmbH + Co. KG devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- 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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