DVR®DORSAL PLATE 131827050Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887868077142), received between Jan 19, 2022 and Jan 19, 2022 — classified as 1 injury.

1 other recall cover devices cleared under the same FDA submission (K140622); 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 18, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryJan 19, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT WAS REVISED APPROXIMATELY ONE-YEAR POST INITIAL IMPLANTATION DUE TO EXTREME PAIN, REDUCED GRIP, AND TROUBLE ROTATING THE LEFT WRIST. NO ADDITIONAL PATIENT CONSEQUENCES WERE REPORTED.

  Patient problems: Loss of Range of Motion; Pain

  MAUDE report 13289073 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K140622. One submission often covers many models, so check the product and lot details in each record.

• Z-1082-2016 · Jan 29, 2016 · Terminated
  Crosslock DVR ePAK -Sterile, Ref 81180050, are complete surgical sets including plates, screws, and instruments for orthopedic fixation The Cross lock DVR ePAK Volar Rim Plates sy