FDANovember 9, 2018device
TEKIA Model 872 Single Piece Hydrophilic Acrylic Intraocular Lenses, Diopter 15.0, Sterile. The firm name on the label is TEKIA, INC., Irvine, CA.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
A limited number of lenses may be mislabeled 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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