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TABLE, HANA, 110 V 6875Recalls & reported problems

Mizuho Orthopedic Systems, Inc. · Class 1

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Quick summary

This Mizuho Hana orthopedic surgical table is a powered operating table used for hip and other orthopedic procedures. The 36 adverse event reports mostly describe patients falling or being dropped during transfers, along with a few cases where the table's cover separated and collapsed while the table was being raised. Reports mention 2 deaths and 26 injuries. No recalls name this device.

AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.

Adverse event reports
36
Deaths reported
2
Injuries reported
27
Recalls naming it
0

Summary

The FDA's MAUDE database contains 36 adverse event reports that list this exact device (DI 00842430108747), received between Dec 5, 2018 and Sep 15, 2026 — classified as 2 deaths, 27 injuries, 7 malfunctions.

The most frequently reported specific device problem is “Use of Device Problem” (15 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

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

Most reported problems

Device problems

  • Use of Device Problem15
  • Insufficient Device Problem Information12
  • Adverse Event Without Identified Device or Use Problem5
  • Improper or Incorrect Procedure or Method4
  • Unintended Movement3
  • Device Fell2
  • Device Handling Problem2
  • Device Slipped1

Patient problems

  • Fall19
  • Insufficient Information5
  • No Clinical Signs, Symptoms or Conditions5
  • Bone Fracture(s)3
  • No Known Impact Or Consequence To Patient3
  • Abrasion2
  • Hematoma2
  • Vertebral Fracture2

Recent adverse event reports

The 25 most recent of 36 reports, in the reporter's own words as published by the FDA.

  • InjurySep 15, 2026Adverse Event Without Identified Device or Use Problem

    A posting from the AHF Podcast (on LinkedIn) highlighted a case where the foot slipped from the boot during a case resulting in a periprosthetic fracture.The patient was reported to be obese and had fit issues with the boot and the foot slipped from the boot under traction leading to a fracture during a revision case. The surgery was completed after resolving the issue.

    Patient problems: Periprosthetic fracture

    MAUDE report 50776603 ↗
  • DeathMay 5, 2026Use of Device Problem; Insufficient Device Problem Information

    AT THE MOMENT OF PATIENT TRANSFER - END OF A CASE, PERINEAL POST AND BELT HAD BEEN REMOVED, BOOTS STILL ATTACHED TO PATIENT. HANA TRANSFER BOARD HAD NOT BEEN PLACED FOR TRANSFER ASSISTANCE. PATIENT WAS LEFT 'UNATTENDED' AND FELL TO THE FLOOR WITH BOOTS STILL ATTACHED. ANESTHESIA TURNED TO DISPOSE OF LMA EQUIPMENT AND PROVIDER SHIFTED TO END OF TABLE TO HELP WITH FEET, STRETCHER WAS PULLED UP TO THE OPPOSITE SIDE OF THE TABLE. PATIENT HAD BEEN IN SCISSOR POSITION FOR DURATION OF CASE.

    Patient problems: Fall; Hematoma; Insufficient Information

    MAUDE report 25088709 ↗
  • InjuryMar 10, 2026Use of Device Problem

    IT WAS REPORTED THAT A PATIENT FELL OFF THE TABLE DURING A CASE. THE REASON OF THE FALL WAS DUE TO THE PERINEAL POST BEING PULLED AFTER THE CASE WITH NO SAFETY STRAPS WHILE THE PATIENT WAS STILL ON THE TABLE.

    Patient problems: Fall

    MAUDE report 24565194 ↗
  • InjuryAug 29, 2025Use of Device Problem; Use of Device Problem

    A PATIENT WAS DROPPED WHILE BEING TRANSFERRED FROM HANA TABLE TO THE TRANSPORT BED. NO INJURIES TO THE PATIENT WERE REPORTED.

    Patient problems: Fall

    MAUDE report 22928699 ↗
  • InjuryNov 15, 2024Insufficient Device Problem Information; Insufficient Device Problem Information

    A PATIENT INJURY INCIDENT WAS REPORTED ON A HANA TABLE.

    Patient problems: Insufficient Information

    MAUDE report 20696241 ↗
  • InjuryOct 30, 2024Use of Device Problem; Use of Device Problem

    A PATIENT FALL FROM HANA ORTHOPEDIC SURGICAL TABLE WAS REPORTED. INSTEAD OF USING THE SAFETY STRAP, A SILK TAPE WAS USED TO SECURE THE PATIENT CAUSING THE FALL.

    Patient problems: Fall

    MAUDE report 20571149 ↗
  • InjurySep 11, 2024Use of Device Problem; Use of Device Problem

    A PATIENT FALL WAS REPORTED WHILE PREPARING FOR THE TRANSFER FROM THE HANA TABLE TO THE GURNEY. THE PATIENT WAS NOT IN THE TRACTION BOOTS, NOT STRAPPED IN AND THE PERINEAL POST WAS REMOVED. THE STAFF WAS NOT PAYING ATTENTION TO THE UNSECURED PATIENT CAUSING THE PATIENT TO FALL. THE FALL CAUSED THE PATIENT'S HEAD TO CRACK AND SUBSEQUENT BLEEDING. THERE WERE NO PROBLEMS WITH THE TABLE ITSELF.

    Patient problems: Head Injury

    MAUDE report 20192910 ↗
  • InjurySep 11, 2024Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information; Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information

    WITHIN 24HRS POST PROCEDURE IT WAS FOUND THAT A PATIENT'S FOOT WAS BROKEN AFTER NOT BEING ABLE TO APPLY PRESSURE TO STAND. THIS PATIENT HAD A DIRECT ANTERIOR HIP PREFORMED, AND ROTATION TO THE FOOT HAD BEEN APPLIED, DEGREE UNKNOWN.

    Patient problems: Bone Fracture(s)

    MAUDE report 20192234 ↗
  • InjuryAug 28, 2024Use of Device Problem; Use of Device Problem

    A PATIENT INJURY THAT OCCURED TWO YEARS AGO WAS REPORTED TO THE MANUFACTURER. THE HOSPITAL PERSONNEL FAILED TO LOCK THE WHEELS OF THE HANA TABLE CAUSING THE PATIENT TO FALL AND EXPERIENCE A BACK INJURY.

    Patient problems: Fall

    MAUDE report 20092545 ↗
  • InjuryJul 24, 2024Use of Device Problem; Use of Device Problem

    PATIENT FELL OFF OF THE HANA TABLE WHILE STILL INTUBATED, THIS WAS AT THE END OF A SURGICAL PROCEDURE. STAFF WAS NOT STANDING NEXT TO THE PATIENT AND THE PATIENT DID NOT HAVE A RESTRAINT STRAP IN POSITION TO HOLD THEM ON THE HANA TABLE, THE PERINEAL POST WAS STILL IN PLACE.

    Patient problems: Aspiration/Inhalation; Fall

    MAUDE report 19818300 ↗
  • InjuryJul 9, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    DURING A DAA THA WITH FEMORAL HEAD AUTOGRAFT ACETABULAR RECONSTRUCTION FOR HIP DYSPLASIA ON A HANA TABLE, THE PATIENT EXPERIENCED PARTIAL VULVAR PRESSURE NECROSIS FROM THE PERINEAL POST. MENTIONED IN RETROSPECTIVE REVIEW OF CASE SERIES "FEMORAL HEAD AUTOGRAFT CAN RELIABLY RECONSTRUCT DYSPLASTIC ACETABULA THROUGH THE DIRECT ANTERIOR APPROACH FOR TOTAL HIP ARTHROPLASTY" BY TAYLOR ET AL IN ARTHROPLASTY TODAY, HTTPS://DOI.ORG/10.1016/J.ARTD.2022.02.005.

    Patient problems: Necrosis; Pressure Sore/Ulcer

    MAUDE report 19705742 ↗
  • InjuryJun 18, 2024Use of Device Problem; Adverse Event Without Identified Device or Use Problem; Use of Device Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT AN ELDERLY FEMALE PATIENT UNDERGOING ANTERIOR HIP ARTHROPLASTY SUFFERED TIBIA FRACTURE WHICH REQUIRED EXTRA SURGERY AND LONGER HOSPITAL STAY. THE TABLE WAS BEING OPERATED BY IMPLANT REP DURING THE SURGICAL PROCEDURE.

    Patient problems: Bone Fracture(s)

    MAUDE report 19558631 ↗
  • InjuryMay 20, 2024Use of Device Problem; Use of Device Problem

    PATIENT BEING TRANSFERRED FROM HANA TABLE TO THE PATIENT BED AFTER SURGERY FELL OFF THE TABLE. THE STAFF DID NOT PUT THE PERINEAL POST IN TO STABILIZE THE PATIENT. SCANS WERE TAKEN TO MAKE SURE THE PATIENT WAS OK AND THE TESTS CAME BACK NEGATIVE. PATIENT HAS SINCE BEEN DECEASED, HOWEVER NOT DUE TO SURGERY OR ANY COMPLICATIONS DUE TO THE FALL.

    Patient problems: Fall

    MAUDE report 19354336 ↗
  • InjuryJan 9, 2024Use of Device Problem; Use of Device Problem

    IT WAS REPORTED THAT DURING A HIP FRACTURE SURGERY, A PATIENT FELL OFF THE TABLE AND THE SAFETY STRAP WAS NOT USED.

    Patient problems: Fall

    MAUDE report 18477829 ↗
  • MalfunctionOct 9, 2023Device Fell; Device Fell

    IT WAS REPORTED THAT THE RIGHT SIDE OF THE HANA TABLE DROPPED DURING THE SURGERY DESPITE IT BEING LOCKED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17901590 ↗
  • InjuryAug 29, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    PATIENT DEVELOPED COMPARTMENT SYNDROME IN BUTTOCK AFTER SURGERY TO REPAIR FEMUR FRACTURE. HANA TABLE WAS USED WITH BILATERAL TRACTION BOOTS AND SCISSORING LEG POSITION. REPORTED IN "CONTRALATERAL GLUTEAL COMPARTMENT SYNDROME AFTER PROLONGED USE OF A FRACTURE TABLE IN A SCISSORING POSITION - A CASE REPORT" BY JENNA GUNN ET AL. JBJS CASE CONNECTOR 13(3):E23.00095, JULY-SEPTEMBER 2023. / DOI: 10.2106/JBJS.CC.23.00095 HTTPS://JOURNALS.LWW.COM/JBJSCC/ABSTRACT/2023/09000/CONTRALATERAL_GLUTEAL_COMPARTMENT_SYNDROME_AFTER.7.ASPX.

    Patient problems: Muscle/Tendon Damage; Swelling/ Edema

    MAUDE report 17647399 ↗
  • InjuryJul 5, 2023Use of Device Problem; Insufficient Device Problem Information; Use of Device Problem; Insufficient Device Problem Information

    IT WAS REPORTED THAT A PATIENT HAD FALLEN OFF A HANA TABLE.

    Patient problems: Fall

    MAUDE report 17262926 ↗
  • InjuryJun 1, 2023Use of Device Problem; Insufficient Device Problem Information; Use of Device Problem; Insufficient Device Problem Information

    AS REPORTED IN FDA MEDWATCH REPORT # MW5117644- "EQUIPMENT MALFUNCTION."

    Patient problems: Limb Fracture; No Clinical Signs, Symptoms or Conditions

    MAUDE report 17043765 ↗
  • MalfunctionSep 1, 2022Unintended System Motion; Unintended System Motion

    IT WAS REPORTED THAT WHEN THE HOSPITAL STAFF WERE TRANSFERRING THE PATIENT TO THE HANA TABLE FOR A SURGERY, THE TABLE ALTHOUGH LOCKED, MOVED AND THEY ALMOST DROPPED THE PATIENT. PATIENT WAS NOT INJURED BUT ONE OF THE EMPLOYEES SUSTAINED A WRIST INJURY.

    Patient problems: Damage to Ligament(s); No Clinical Signs, Symptoms or Conditions

    MAUDE report 15342068 ↗
  • InjuryAug 8, 2022Insufficient Device Problem Information; Device Handling Problem; Insufficient Device Problem Information; Device Handling Problem

    IT WAS REPORTED THAT THE TOP OF THE TABLE MOVED 2 PLUS INCHES IN AN AIRPLANE FASHION DURING SURGERY. THE PATIENT FELL OFF THE BED AND SUSTAINED INJURY.

    Patient problems: Abrasion; Bruise/Contusion; Fall; Insufficient Information; Laceration(s); Vertebral Fracture

    MAUDE report 15189157 ↗
  • InjuryJun 8, 2022Insufficient Device Problem Information; Insufficient Device Problem Information

    IT WAS REPORTED THAT A PATIENT FELL FROM THE TABLE AFTER SURGERY.

    Patient problems: Fall

    MAUDE report 14640368 ↗
  • InjuryMay 4, 2022No Apparent Adverse Event; Insufficient Device Problem Information; No Apparent Adverse Event; Insufficient Device Problem Information

    IT WAS REPORTED THAT A PATIENT MAY HAVE FALLEN OR ALMOST FALLEN OFF AN OPERATING TABLE.

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

    MAUDE report 14284236 ↗
  • InjuryMar 8, 2022Use of Device Problem; Use of Device Problem

    THE PATIENT WAS SUPINE ON THE TABLE AND SLID OFF. THE SAFETY STRAP WAS NOT BEING USED. NO INJURIES.

    Patient problems: Fall

    MAUDE report 13695216 ↗
  • InjuryJan 14, 2022Use of Device Problem; Use of Device Problem

    DURING SURGERY FOR HIP FRACTURE PATIENT SLID OFF THE TABLE AND FELL ON TOP OF THE SURGEON. NEITHER WAS INJURED. THE SAFETY STRAP WAS NOT BEING USED. PATIENT WITH BMI OVER 40 WAS PARTIALLY TAPED TO THE TABLE. WITH A DIFFICULT REDUCTION, PULLING TRACTION AND PUSHING ON PATIENT, THE TAPE GAVE WAY AND THE PATIENT SLID. THE PATIENT WAS SCANNED AND THE SURGERY RESCHEDULED FOR ANOTHER DAY, WHEN IT WAS COMPLETED SUCCESSFULLY WITH A SAFETY STRAP IN PLACE.

    Patient problems: Fall

    MAUDE report 13259184 ↗
  • MalfunctionNov 16, 2021Device Fell; Device Fell

    IN THE MIDDLE OF SURGERY THE LEG JOINT LOCK BROKE AND IT FELL TO THE FLOOR.

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

    MAUDE report 12820749 ↗

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