Restor3d recalls

Restor3d appears in 4 official U.S. recall notices indexed by RecallRadar, most recently on 2026-08-26.

Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.

• Brand Name: Veritas Standard Reverse Total Shoulder Product Name: Veritas Standard Glenoid Baseplate Model/Catalog Number: 1500-1030
  FDA Device · Class II · 2026-08-26 · Restor3d
• Non-Sterile Double Ended Trial Kit, Small Footprint, (6110-N01-KTS01) for the Cervical Cage
  FDA Device · Class II · 2022-05-11 · Restor3d
• Evans Wedge Disposable Trials, Medium Footprint, 10mm Thickness (6101-20181018)
  FDA Device · Class II · 2022-05-11 · Restor3d
• Evans Wedge Disposable Trials, Large Footprint, 8mm Thickness (Model: 6101-22200818)
  FDA Device · Class II · 2022-05-11 · Restor3d