Volar Bearing Plates VLBPL-7-7Recalls & reported problems
Trimed, INC. · VolarBearingPlate,Lt,7-Hole,7-Peg · Class 2 · Implant
All models of Volar Bearing Plates (16)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00842188101595), received between Oct 24, 2024 and Oct 24, 2024 — classified as 1 injury.
The most frequently reported specific device problem is “Deformation Due to Compressive Stress” (1 report).
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
- Deformation Due to Compressive Stress1
Patient problems
- Fall1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryOct 24, 2024Deformation Due to Compressive Stress; Deformation Due to Compressive Stress
A REGIONAL SALES MANAGER REPORTED ON 25SEP2024 THAT A REP REPORTED THAT A SURGEON IMPLANTED A TRIMED PLATE (DATE UNKNOWN) AND AFTER THE PATIENT FELL, THEIR RADIUS BROKE PROXIMAL TO THE PLATE. THIS LED TO A REVISION SURGERY (DATE UNKNOWN) AND LARGER PLATE, VLBPL-7-7 WAS IMPLANTED. IT WAS STATED THAT AFTER THE REVISION SURGERY, THE PATIENT FELL AGAIN AND BENT PLATE. ON (B)(6) 2024 THE PLATE WAS REMOVED AND DISCOLORATION OF BONE AND TISSUE WAS EVIDENT. THE SURGEON STATED THAT IT HAD SIMILAR APPEARANCE TO METALOSIS. THE SURGEON ULTIMATELY CHOSE TO IMPLANT ANOTHER PLATE FROM A COMPETITOR. PICTURES WERE PROVIDED, X-RAYS WERE REQUESTED BUT NOT PROVIDED AND THE DEVICE WAS DISCARDED BY THE FACILITY. AS OF 24OCT2024 TRIMED CONTINUES TO REQUEST INFORMATION FROM THE REP TO CLARIFY TIMELINES AND INFORMATION PROVIDED BY THE REGIONAL SALES MANAGER AND THE SALES REP.
Patient problems: Fall
MAUDE report 20528418 ↗
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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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