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.
Recall summary
| Recall notices | 2 |
|---|---|
| Published | 2015-11-18 to 2019-12-25 |
| By agency | FDA Device (2) |
| By classification | Class II (2) |
| By status | terminated (2) |
Recalls
- TEKIA Model 872 Single Piece Hydrophilic Acrylic Intraocular Lenses, Diopter 15.0, Sterile
FDA Device · Class II · 2019-12-25 · Tekia
Reason: A limited number of lenses may be mislabeled with the incorrect diopter power. - TEKIA Single Piece Hydrophilic Acrylic Intraocular Lenses, Model 811
FDA Device · Class II · 2015-11-18 · Tekia
Reason: Tekia is recalling the Single Piece Hydrophillic Acrylic Intraocular Lenses (IOLs) because they may be labeled with the incorrect diopter power.