VOLT" Wrist Treatment System 2.4/2.7 2Column Dist Radius Plate 6Hd/14Shaft/Left/Std/186mm recall — FDA Z-1132-2026
The supplier manufactured anatomical left plates with an incorrect thread orientation.
Overview of recall records associated with Tyber Medical, including dates, categories and classifications where available.
Classification mix: Class II: 2.
The supplier manufactured anatomical left plates with an incorrect thread orientation.
The supplier manufactured anatomical left plates with an incorrect thread orientation.
This page summarizes recall records in which the official source identifies Tyber Medical as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.