Volar Bearing Plates VBEAL-3-7NRecalls & reported problems
Trimed, INC. · Volar Bearing Plate, 3-Hole, Lt, Narrow · Class 2 · Implant
All models of Volar Bearing Plates (16)
Data updated Oct 18, 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
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00842188124907), received between Nov 28, 2023 and Nov 28, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (1 report).
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 18, 2026.
Reports received per month
Recalls naming this device
- Nov 28, 2023Class IIOpen, Classified
Plates, part of a wrist fixation system, are affixed during surgery with bearings that may pop out from distal peg holes.
Z-0932-2024 · Root cause: Labeling design · Recall details · FDA record ↗
Most reported problems
Device problems
- Detachment of Device or Device Component1
- Off-Label Use1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 28, 2023Off-Label Use; Detachment of Device or Device Component; Off-Label Use; Detachment of Device or Device Component
TRIMED'S MEDICAL ADVISOR REPORTED ON 05NOV2023 THAT A SURGEON INFORMED HIM THAT ON ONE CASE, HE WAS USING A WRIST FIXATION SYSTEM 3 VOLAR BEARING PLATE AND USED A STANDARD BONE SCREW TO PULL THE PLATE UP TO THE BONE. THIS IS NOT ON THE TRIMED SURGICAL TECHNIQUE MANUAL, THEREFORE THIS WAS OFF LABEL USE. WHEN THE SURGEON WENT TO PUT THE PEG IN, HE THINKS THAT THE BEARING MAY HAVE COME OUT OF THE BOTTOM OF THE PLATE, BUT FELT THAT FIXATION WAS EXCELLENT, WAS PLEASED WITH THE RESULT, AND DIDN'T FEEL REMOVAL WAS NEEDED OR NECESSARY. IT HAS BEEN REPORTED THAT THE PATIENT HAS DONE GREAT AND THIS DID NOT CAUSE ADDITIONAL HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18223020 ↗
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- PRECICE® Plating System LP4.5-PLF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls3 reports
- PRECICE® Plating System LP4.5-DRF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls1 report
- PRECICE® Plating System LP4.5-MLT42Nuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls0 reports
- PRECICE® Plating System LP4.5-MRT42Nuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls0 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 · each recall links to the FDA recall notice
- 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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