Trumpf Medical 4080100Recalls & reported problems
Baxter Medical Systems GmbH + Co. KG · PST 500 · Class 2
All models of TRUMPF MEDICAL (11)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 9
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 00887761979390), received between Jun 23, 2021 and Aug 14, 2026 — classified as 9 malfunctions.
The most frequently reported specific device problem is “Unintended Movement” (4 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
- Unintended Movement4
- Unstable4
- Device Slipped1
- Operating System Becomes Nonfunctional1
Patient problems
- No Clinical Signs, Symptoms or Conditions9
Recent adverse event reports
The 9 most recent of 9 reports, 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 ↗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 ↗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 ↗MalfunctionAug 9, 2024Operating System Becomes Nonfunctional; Operating System Becomes Nonfunctional
CUSTOMER REPORTED THAT TABLE HAS NO FUNCTIONS. DISPLAYING ERROR 62. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT # (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19951035 ↗MalfunctionFeb 20, 2024Unstable; Unstable
CUSTOMER REPORTED THAT AFTER SOME TIME HYDRAULIC STAMPS DISENGAGE. IT WAS STATED THAT USUALLY ONLY ONE STAMP LOOSE PRESSURE AND TABLE WILL LOOSE LEVEL AND START MOVING ON THAT ONE STAMP. NO HARM OR SIGNIFICANT IMPACT TO THE SURGICAL PROCEDURE 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 18743751 ↗MalfunctionMar 27, 2023Device Slipped; Device Slipped
CUSTOMER REPORTED THAT HYDRAULIC UNIT AFTER SOME TIME DISENGAGES (LOSS OF PRESSURE) WITHOUT TABLE RECOGNIZING ITS UNLOCKED. STAFF THEN HAVE TO UNLOCK THE TABLE SO SOFTWARE WILL KNOW ITS UNLOCKED (WITHOUT ANY EFFECT BECAUSE BRAKES ARE ALREADY UNLOCKED) AND THEN LOCK IT AGAIN. ADDITIONALLY IT WAS CONFIRMED THAT ALL FOUR STAMPS RELEASED DURING PROCEDURES AND THEN THE TABLE MOVES WHEN SOMEONE IS LEANING ON IT. NO HARM OR SIGNIFICANT IMPACT TO THE SURGICAL PROCEDURE 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 16618636 ↗MalfunctionSep 8, 2021Unstable; Unstable
THE CUSTOMER REPORTED THE OPERATING TABLE WAS ON THE BRAKES WHEN STARTING THE SURGICAL PROCEDURE. AFTER TEN MINUTES TWO BRAKES RELEASED AND THE DEVICE WAS ROCKING. NO HARM OR SIGNIFICANT IMPACT TO THE SURGICAL PROCEDURE 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 12437992 ↗MalfunctionJun 23, 2021Unstable; Unintended Movement; Unstable; Unintended Movement
IT WAS REPORTED, DURING A VERY PRECISE SURGICAL PROCEDURE THE OPERATING TABLE BECAME UNSTABLE (TILTING). NO HARM OR SIGNIFICANT IMPACT TO THE SURGICAL PROCEDURE 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 12048378 ↗
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- TS 7500 1730720Baxter Medical Systems GmbH + Co. KG · Table, radiologic1 recall1 report
- TS 7500 1854086Baxter Medical Systems GmbH + Co. KG · Table, radiologic1 recall0 reports
- TS 7500 1730732Baxter Medical Systems GmbH + Co. KG · Table, radiologic1 recall0 reports
- NA 6265300-20GE Medical Systems, L.L.C. · Table, radiologic1 recall0 reports
- TS 7000 1604786Baxter Medical Systems GmbH + Co. KG · Table, radiologic1 recall0 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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