Volar Bearing Plates VBEAL-3-7WRecalls & reported problems
Trimed, INC. · Volar Bearing Plate, 3-Hole, Lt, Wide · 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
- 1
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00842188124969), received between Sep 30, 2024 and Sep 30, 2024 — classified as 1 injury.
The most frequently reported specific device problem is “Break” (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
- Break1
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.
InjurySep 30, 2024Break; Break
SALES REP REPORTED ON 28AUG2024 THAT A SURGEON EXPERIENCED A BEARING POPPED OUT OF A VBEAL-3-7W. IT WAS REPORTED THAT THE SURGEON CHOSE TO LEAVE THE DEVICE IMPLANTED WITHOUT THE BEARING AND THE REP DOES NOT BELIEVE THIS WILL CAUSE THE PATIENT ADDITIONAL HARM. THE REP REPORTED THAT THERE WAS ABOUT A 45-MINUTE DELAY IN SURGERY DUE TO HAVING TO REMOVE THE LOOSE BEARING FROM BEHIND THE PLATE. THE REP ALSO REPORTED THAT THERE IS CURRENTLY NO REPORTED ADVERSE EVENT. NO DEVICE IS AVAILABLE TO BE RETURNED BUT X-RAYS AND A PICTURE WERE PROVIDED. WHEN INITIALLY REVIEWING THE COMPLAINT, WE SAW THAT IT SAID THE SURGEON INDICATED NO ADDITIONAL HARM; HOWEVER, THE DELAY IN SURGERY WAS OVERLOOKED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20340762 ↗
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- PRECICE® Plating System LP4.5-MRT4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls3 reports
- 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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