FDASeptember 29, 2015device
TEKIA Single Piece Hydrophilic Acrylic Intraocular Lenses, Model 811
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Tekia is recalling the Single Piece Hydrophillic Acrylic Intraocular Lenses (IOLs) because they may be labeled with the incorrect diopter power.
What to do
FDA enforcement status: Terminated
Brands named
tekia
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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