Tekia recalls

Tekia appears in 2 official U.S. recall notices indexed by RecallRadar, most recently on 2019-12-25.

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

• TEKIA Model 872 Single Piece Hydrophilic Acrylic Intraocular Lenses, Diopter 15.0, Sterile
  FDA Device · Class II · 2019-12-25 · Tekia
• TEKIA Single Piece Hydrophilic Acrylic Intraocular Lenses, Model 811
  FDA Device · Class II · 2015-11-18 · Tekia