Class II — Tekia, Inc.
| Recalling firm | TEKIA, INC |
|---|---|
| Registered facility | TEKIA, INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Tekia is recalling the Single Piece Hydrophillic Acrylic Intraocular Lenses (IOLs) because they may be labeled with the incorrect diopter power. |
| Product | TEKIA Single Piece Hydrophilic Acrylic Intraocular Lenses, Model 811 |
| Quantity | 50 units |
| Distribution | Internationally to Vietnam. |
| Initiated | 2015-09-29 |
| Classified | 2015-11-06 |
| Terminated | 2015-12-03 |
| Recall number | Z-0237-2016 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Tekia, Inc. (Z-0237-2016).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/72434/
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