TEKIA, INC
2 recall(s) on record — most severe on record: Class II.
Recalls by year
- Recalls (2)
Registered facilities (1)
- TEKIA, INC. FEI 3002023310 · CA
Recalls & enforcement
- Class IITerminated2018-11-09A limited number of lenses may be mislabeled with the incorrect diopter power.
- Class IITerminated2015-09-29Tekia is recalling the Single Piece Hydrophillic Acrylic Intraocular Lenses (IOLs) because they may be labeled with the incorrect diopter power.
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.
Cite this record
RegWarden. “TEKIA, INC — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-10023535-tekia-inc/
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