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TRIOS, TABLE BASE 7803Recalls & reported problems

Mizuho Orthopedic Systems, Inc. · Class 1

Adverse event reports
8
Deaths reported
0
Injuries reported
3
Recalls naming it
0

Summary

The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 00842430103957), received between Sep 4, 2019 and Jan 19, 2026 — classified as 3 injuries, 5 malfunctions.

The most frequently reported specific device problem is “Use of Device Problem” (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. How this data works · Data updated Oct 13, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 1 reportsJul 2024: 0 reportsAug 2024: 2 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 1 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520262
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Use of Device Problem4
  • Unintended Movement2
  • Adverse Event Without Identified Device or Use Problem1
  • Device Dislodged or Dislocated1
  • Improper or Incorrect Procedure or Method1
  • Insufficient Device Problem Information1
  • Unintended System Motion1

Patient problems

  • Fall4
  • No Clinical Signs, Symptoms or Conditions4
  • Unintended Extubation2
  • Insufficient Information1
  • Laceration(s)1
  • No Known Impact Or Consequence To Patient1
  • Paraplegia1
  • Respiratory Insufficiency1

Recent adverse event reports

The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJan 19, 2026Unintended Movement

    CLINICIAN REPORTS THAT THE TABLE KEPT TILTING WITH PATIENT ON THE TABLE. ERROR CODES 1048 AND 220 C REPORTED. EVALUATION REQUIRED TO DETERMINE THE ISSUE.

    Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions

    MAUDE report 24110650 ↗
  • MalfunctionAug 29, 2024Use of Device Problem; Insufficient Device Problem Information; Use of Device Problem; Insufficient Device Problem Information

    A PATIENT FELL DURING THE TRANSFER FROM THE OPERATING TABLE BACK TO THE HOSPITAL BED. THE FRAME WAS SUSPECTED TO BE UNLOCKED WHICH CAUSED THE PATIENT TO FALL AND HIT THE FLOOR.

    Patient problems: Fall; No Clinical Signs, Symptoms or Conditions

    MAUDE report 20102414 ↗
  • MalfunctionAug 14, 2024Unintended System Motion; Unintended System Motion

    WHILE PATIENT WAS ON THE TABLE, THE TRIOS TABLE SYSTEM BEGAN SHAKING OR "SPUTTERING" UNCONTROLLABLY. THE SPUTTERING WAS EXCESSIVE ENOUGH DURING THIS LATEST EPISODE THAT THE TEAM IN THE ROOM THOUGHT THE PATIENT MAY FALL OFF THE TABLE. SPUTTERING OCCURED INTERMITTENTLY UNTIL IT GOT TO 39 INCHES AND UP WHEN IT BECAME ITS WORST.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 19982449 ↗
  • InjuryJun 12, 2024Use of Device Problem; Use of Device Problem

    IT WAS REPORTED THAT A WOMAN FELL FROM THE TRIOS TABLE WHEN IT WAS TILTED. SHE WASN'T STRAPPED AROUND THE TOP. THE TABLE WAS BARELY TILTED WHEN SHE FELL OFF AND HIT HER HEAD. A COUPLE DAYS LATER DOCTORS TOLD THE FSE THAT IT WASN'T A JERK BUT SLIGHT MOVEMENT IN THE HEAD IN ASSEMBLY. FSE TOLD THEM MAXIMUM MOVEMENT IS TWO DEGREES (CLOCKWISE AND COUNTERCLOCKWISE) AND IT MEASURED AROUND 1 AT THE TIME OF INSPECTION SO IT IS FINE.

    Patient problems: Fall

    MAUDE report 19525178 ↗
  • InjuryJan 24, 2023Use of Device Problem; Improper or Incorrect Procedure or Method; Use of Device Problem; Improper or Incorrect Procedure or Method

    PROCEDURE WAS T5 TO T10 LAMINECTOMY WITH MICROSCOPIC DISSECTION AND TUMOR RESECTION. PATIENT WAS PRONE, LOWER BODY SECURED TO TABLE. THE TABLE WAS AIRPLANED TO IMPROVE SURGICAL ACCESS. PATIENT SLID OFF THE TABLE ONTO THE FLOOR.

    Patient problems: Fall; Laceration(s); Paraplegia; Respiratory Insufficiency; Unintended Extubation

    MAUDE report 16238013 ↗
  • InjuryApr 20, 2022Use of Device Problem; Adverse Event Without Identified Device or Use Problem; Use of Device Problem; Adverse Event Without Identified Device or Use Problem

    AN INCIDENT OF PATIENT FALLING FROM THE TABLE WAS REPORTED. AN OPERATIONAL CHECK OF THE TABLE WAS PERFORMED WHICH CONCLUDED HAVING NO PROBLEM WITH THE TABLE. IT WAS REPORTED BY OR LEAD COORDINATOR THAT ONE OF THE NURSES HAD PUT SOME FOOT BOARDS ON THE TABLE WHICH CAUSED THE INCIDENT OF PATIENT FALL. THIS WAS DEEMED AS OPERATOR'S ERROR WITH NO REPORTS OF PATIENT INJURY.

    Patient problems: Fall; Unintended Extubation

    MAUDE report 14161950 ↗
  • MalfunctionFeb 25, 2021Unintended Movement; Unintended Movement

    IT WAS REPORTED TABLETOP STARTED TILTING AT THE END OF THE PROCEDURE, LUCKILY THE NURSE CAUGHT THE PATIENT BEFORE HE/SHE FELL.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11377827 ↗
  • MalfunctionSep 4, 2019Device Dislodged or Dislocated; Device Dislodged or Dislocated

    USING A TRIOS SURGICAL TABLE THE CUSTOMER WAS USING THE EXTENDABLE TRACTION UNIT TO APPLY 15LBS OF WEIGHT TO THE PATIENTS HEAD. A HOSPITAL STAFF MEMBER ACCIDENTALLY PRESSED THE RELEASE BUTTON FOR THE TRACTION ASSEMBLY CAUSING IT TO RETRACT AND DROPPING THE WEIGHTS ABOUT 4IN. I AM TOLD THAT IF A DOCTOR WASN'T HOLDING THE PATIENTS HEAD IT COULD HAVE BEEN A SERIOUS ISSUE. FROM WHAT I WAS TOLD THERE WAS NO INJURIES CAUSED TO THE PATIENT.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 8961685 ↗

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.