MULTILOK TABLE BASE 0302-001Recalls & reported problems
Mizuho Orthopedic Systems, Inc. · Class 1
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00842430111167), received between Jul 14, 2020 and Jul 14, 2020 — classified as 2 injuries.
The most frequently reported specific device problem is “Failure to Eject” (2 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.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem2
- Failure to Eject2
Patient problems
- Injury2
- Needle Stick/Puncture2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJul 14, 2020Adverse Event Without Identified Device or Use Problem; Failure to Eject; Adverse Event Without Identified Device or Use Problem; Failure to Eject
STAFF WAS DISMANTLING STERILE FIELD POST PROCEDURE. WHEN DISENGAGING THE HAND TABLE TOP FROM THE BASE THE DISPOSABLE TOP PUNCTURED THROUGH THE STAFF'S GLOVES. SHE NOTICED THREE PUNCTURE HOLES THROUGH HER LEFT FIFTH FINGER. WENT TO EMERGENCY AND RECEIVED HEPATITIS C PROPHYLAXIS. SUBSEQUENT INFORMATION RECEIVED FROM THE FACILITY INDICATED THERE WAS SOME DIFFICULTY REMOVING THE (CORIN) TOP FROM THE (MIZUHO OSI) BASE WHICH CONTRIBUTED TO THE PROBLEM.
Patient problems: Injury; Needle Stick/Puncture
MAUDE report 10271279 ↗InjuryJul 14, 2020Adverse Event Without Identified Device or Use Problem; Failure to Eject; Adverse Event Without Identified Device or Use Problem; Failure to Eject
A STAFF MEMBER HAD DIFFICULTY RELEASING A HAND TABLE TOP FROM THE BASE AND WAS INJURED BY A SHARP EDGE ON THE TOP.
Patient problems: Injury; Needle Stick/Puncture
MAUDE report 10271203 ↗
Other Table, Operating-Room, Mechanical devices
- Hip Instruments 01.15.10.0190Medacta International SA · Table, Operating-Room, Mechanical8 reports
- HIP Instruments 01.15.10.0315Medacta International SA · Table, Operating-Room, Mechanical3 reports
- Hip Instruments 01.15.10.0071Medacta International SA · Table, Operating-Room, Mechanical1 report
- Hip Instruments 01.15.10.0321Medacta International SA · Table, Operating-Room, Mechanical1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.