TS 7000 1723633Recalls & reported problems
Baxter Medical Systems GmbH + Co. KG · Operating table TruSystem 7000 U (dV) · Class 1
All models of TS 7000 (3)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 22
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 22 adverse event reports that list this exact device (DI 00887761967519), received between May 8, 2023 and Sep 25, 2026 — classified as 1 injury, 21 malfunctions.
The most frequently reported specific device problem is “Unintended Movement” (6 reports).
1 FDA recall record name this device's identifier, 1 still open.
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 16, 2026.
Reports received per month
Recalls naming this device
- Sep 19, 2024Open, Classified
The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.
Z-0210-2025 · Root cause: Device Design · Recall details · FDA record ↗
Most reported problems
Device problems
- Unintended Movement6
- Key or Button Unresponsive/not Working5
- Operating System Becomes Nonfunctional5
- Device Fell2
- Positioning Failure2
- Arcing1
- Fire1
- Material Split, Cut or Torn1
Patient problems
- No Clinical Signs, Symptoms or Conditions20
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
- Bruise/Contusion1
Recent adverse event reports
The 22 most recent of 22 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 25, 2026Unintended Movement
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50900045 ↗MalfunctionSep 10, 2026Unintended System Motion
Baxter received a report that Operating table TruSystem 7000 U (dV) had table will move without any control button press. The process step during which this occurred was unknown. There was no patient/user injury, medical intervention, symptom, or adverse event reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50703689 ↗MalfunctionApr 10, 2026Unstable
BAXTER RECEIVED A REPORT THAT OR TABLE TRUSYSTEM 7000 U HAD WOBBLE MOVEMENT WHEN BRAKES ENGAGE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24840651 ↗MalfunctionMar 11, 2026Key or Button Unresponsive/not Working
BAXTER RECEIVED A REPORT STATING THAT OPERATING TABLE TRUSYSTEM 7000 WAS WOBBLY. THERE WAS NO INJURY, DEATH, OR PROCEDURAL DELAY REPORTED WITH THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24568115 ↗MalfunctionMar 11, 2026Key or Button Unresponsive/not Working
BAXTER RECEIVED A REPORT STATING THAT DURING SURGICAL PROCEDURE, OR TABLE TRUSYSTEM 7000 U (DV) WAS UNABLE TO BE ACTIVATING. NO OPERATION WAS POSSIBLE FROM THE REMOTE CONTROL AND THE COLUMN KEYPAD. USER TRIED EMERGENCY OVERRIDE AND POWERED OFF TABLE SEVERAL TIMES WITH NO CHANGE. THERE WAS NO INJURY, DEATH, OR PROCEDURAL DELAY REPORTED WITH THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24568061 ↗MalfunctionMar 10, 2026Key or Button Unresponsive/not Working
BAXTER RECEIVED A REPORT STATING THAT OPERATING TABLE TRUSYSTEM 7000 WAS NOT PROVIDING ANY FUNCTION WHILE ACTIVATING. THE BED WAS LOCATED AT THE ACCOUNT. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24561332 ↗MalfunctionMar 6, 2026Positioning Failure; Key or Button Unresponsive/not Working
BAXTER RECEIVED A REPORT STATING THAT OR TABLE TRUSYSTEM 7000 U (DV) WAS STUCK IN TRENDLEBURG AND NO FUNCTION WAS POSSIBLE TO ACTIVATE. CUSTOMER TRIED RESETTING TABLE BUT THIS DID NOT RESOLVE THE ISSUE. THERE WAS NO INJURY, DEATH, OR PROCEDURAL DELAY REPORTED WITH THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24536036 ↗MalfunctionFeb 3, 2026Positioning Failure; Mechanical Problem
BAXTER RECEIVED A REPORT STATING THAT DURING A PROCEDURE, A OPERATING TABLE TRUSYSTEM 7000 WAS STUCK IN TREND MODE AND WAS UNABLE TO MOVE THE TABLE. REMOTE SCREEN IS BLACK AND ON BUTTON IS FLASHING. 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 24248028 ↗MalfunctionNov 18, 2025Unintended Movement; Device Fell; Unintended Movement; Device Fell
BAXTER RECEIVED A REPORT STATING THAT OPERATING TABLE TRUSYSTEM 7000 (PRODUCT CODE 1723633, SERIAL NUMBER (B)(6)), WAS IN REVERSE TRENDELENBURG POSITION, THE TABLE SLID DOWNWARD AND THE FOOT END OF THE TABLE ¿CRUSHED A NURSE¿S FOOT¿. THE NURSE WAS SEEN IN THE EMERGENCY DEPARTMENT, AND IT WAS REPORTED THE NURSE HAD A BRUISED FOOT.
Patient problems: Bruise/Contusion
MAUDE report 23585966 ↗MalfunctionAug 26, 2025Sparking; Material Split, Cut or Torn; Sparking; Material Split, Cut or Torn
BAXTER RECEIVED A REPORT STATING THAT OPERATING TABLE TRUSYSTEM 7000 PLUG-IN PORT WAS RIPPED AND COMPLETELY UNHOUSED, GENERATING SOME SPARKS WHEN PLUGGED IN. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22896528 ↗MalfunctionAug 21, 2025Unintended Movement; Unintended Movement
BAXTER RECEIVED A REPORT STATING THAT OPERATING TABLE TRUSYSTEM 7000 WAS UNLOCKING IN THE MIDDLE OF THE PROCEDURE. NO HARM OR SIGNIFICANT IMPACT TO THE SURGICAL PROCEDURE WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22862537 ↗MalfunctionAug 5, 2025Unintended Movement; Device Fell; Unintended Movement; Device Fell
BAXTER RECEIVED A REPORT STATING THAT DURING A PROCEDURE, WHEN PUTTING THE PATIENT IN REVERSE TREND, OPERATING TABLE TRUSYSTEM 7000 FOOT SIDE DROPPED SUDDENLY. NO HARM OR SIGNIFICANT IMPACT TO THE SURGICAL PROCEDURE WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22716178 ↗MalfunctionJul 24, 2025Unintended Movement; Unintended Movement
BAXTER RECEIVED A REPORT STATING THAT OPERATING TABLE TRUSYSTEM 7000 UNLOCKED ON ITS OWN DURING PROCEDURE. NO HARM OR SIGNIFICANT IMPACT TO THE SURGICAL PROCEDURE WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22591356 ↗MalfunctionJul 22, 2025Unintended Movement; Unintended Movement
BAXTER RECEIVED A REPORT STATING THAT OPERATING TRUSYSTEM 7000 TABLE FLOOR LOCKS UNLOCKED DURING A CASE. NO HARM OR SIGNIFICANT IMPACT TO THE SURGICAL PROCEDURE WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22567218 ↗MalfunctionMar 6, 2025Operating System Becomes Nonfunctional; Operating System Becomes Nonfunctional
CUSTOMER REPORTED TABLE WAS UNRESPONSIVE ON KEYPAD AND REMOTE DURING SURGERY. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT # (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21536693 ↗MalfunctionFeb 26, 2025Operating System Becomes Nonfunctional; Operating System Becomes Nonfunctional
CUSTOMER REPORTED TABLE IS GETTING ERROR 904 AND NO FUNCTIONS ARE WORKING. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT # (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21468254 ↗MalfunctionFeb 25, 2025Operating System Becomes Nonfunctional; Operating System Becomes Nonfunctional
CUSTOMER REPORTED TABLE HAS STOPPED FUNCTIONING. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT #(B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21458753 ↗MalfunctionJan 29, 2025Operating System Becomes Nonfunctional; Operating System Becomes Nonfunctional
CUSTOMER REPORTED BED IS STUCK AND THEY ARE UNABLE TO MOVE IT. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT #(B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21262346 ↗MalfunctionJan 6, 2025Arcing; Arcing
THE CUSTOMER REPORTED A SMALL FIRE FROM THE POWER CORD. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT #(B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21078073 ↗MalfunctionNov 21, 2024Operating System Becomes Nonfunctional; Operating System Becomes Nonfunctional
CUSTOMER REPORTED TABLE LOST ALL FUNCTIONS. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT # (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20745391 ↗MalfunctionSep 30, 2024Key or Button Unresponsive/not Working; Key or Button Unresponsive/not Working
THE CUSTOMER REPORTED THAT THE BED WAS NOT MOVING. 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 20333740 ↗InjuryMay 8, 2023Fire; Fire
THE CUSTOMER REPORTED THE TRUSYSTEM 7000 OPERATING TABLE CAUGHT ON FIRE LEADING TO SMOKE IN THE OPERATING ROOM (OR) WHILE A PATIENT WAS ON THE TABLE. IN THIS EVENT, A SCRUB TECH REPORTED DIFFICULTY BREATHING AT THE TIME OF THE EVENT AND REQUIRED MEDICAL INTERVENTION (USE OF INHALERS) TO PRECLUDE PERMANENT IMPAIRMENT OF BODY FUNCTION OR PERMANENT DAMAGE TO BODY STRUCTURE. THE EVENT WAS TEMPORARILY LIFE THREATENING TO THE PATIENT AND CAREGIVERS EXPOSED TO THE FIRE AND SMOKE (POTENTIALLY OXYGEN RICH ENVIRONMENT AND/OR FLAMMABLE GASES PRESENT), AND THEREFORE, WILL BE CONSIDERED A SERIOUS INJURY. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT #(B)(4).
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 16885412 ↗
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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 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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