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
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 ↗
Other Table, Surgical With Orthopedic Accessories, Ac-Powered devices
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- TS 7500 1854085Baxter Medical Systems GmbH + Co. KG · TABLE, SURGICAL WITH ORTHOPEDIC ACCESSORIES, AC-POWERED1 recall0 reports
- TS 7500 1854087Baxter Medical Systems GmbH + Co. KG · TABLE, SURGICAL WITH ORTHOPEDIC ACCESSORIES, AC-POWERED1 recall0 reports
- ADVANCED CONTROL I-BASE, DC 5803Mizuho Orthopedic Systems, Inc. · Table, Surgical With Orthopedic Accessories, Ac-Powered47 reports
- TRUMPF MEDICAL 1723633Baxter Medical Systems GmbH + Co. KG · TABLE, SURGICAL WITH ORTHOPEDIC ACCESSORIES, AC-POWERED43 reports
- Levó Arm 7887-050Mizuho Orthopedic Systems, Inc. · Table, Surgical With Orthopedic Accessories, Ac-Powered12 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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