Volar Fixed Angle Plates VPPL-5-7Recalls & reported problems
Trimed, INC. · Volar Fixed Angle Plate, Lt, 5-Hole, 7-Peg · Class 2 · Implant
Data updated Oct 16, 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 00842188101755), received between Nov 16, 2021 and Nov 16, 2021 — classified as 1 injury.
The most frequently reported specific device problem is “Break” (1 report).
1 other recall cover devices cleared under the same FDA submission (K951302); they may or may not involve this specific model.
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 16, 2026.
Most reported problems
Device problems
- Break1
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.
InjuryNov 16, 2021Break; Break
A TRIMED SALES REPRESENTATIVE REPORTED ON (B)(6) 2021 THAT A BROKEN VPPL-5-7 WAS REMOVED FROM THE PATIENT. THE PATIENT HAD FALLEN AND BROKE THE PLATE. THE INITIAL IMPLANTATION OF THE VPPL-5-7 WAS ON (B)(6) 2021, THE FALL AND REMOVAL OCCURRED SOMETIME IN (B)(6). IT IS BELIEVED THAT PRIOR TO THE FALL, THE PATIENT WAS HEALING WELL FROM THE INITIAL SURGERY. THE PLATE AND SCREWS WERE REMOVED AND REPLACED WITH BONE GRAFT MATERIAL AS WELL AS PINS TO ACHIEVE FIXATION. IT IS CURRENTLY BELIEVED THAT THE PATIENT IS HEALING WELL. INSPECTION OF THE DEVICE FOUND THAT THE DEVICE LIKELY BROKE DUE TO THE IMPACT FROM THE FALL AND DEVICE DID NOT MALFUNCTION DUE TO MATERIAL INTEGRITY.
Patient problems: Fall
MAUDE report 12820458 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K951302. One submission often covers many models, so check the product and lot details in each record.
- Z-0118-2020 · Aug 24, 2018 · TerminatedTriMed Dorsal Wrist Hook Plate, Dorsal, 4-Hole, REF WHD-4, contained in a tray, insert, or poly package containing varying amounts, Nonsterile, Single Use Only, Rx. The firm name
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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