Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

TEKIA Single Piece Hydrophilic Acrylic Intraocular Lenses Recalled by Tekia, Inc. Due to Tekia is recalling the Single Piece Hydrophillic Acrylic...

Date: September 29, 2015
Company: Tekia, Inc.
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Tekia, Inc. directly.

Affected Products

TEKIA Single Piece Hydrophilic Acrylic Intraocular Lenses, Model 811

Quantity: 50 units

Why Was This Recalled?

Tekia is recalling the Single Piece Hydrophillic Acrylic Intraocular Lenses (IOLs) because they may be labeled with the incorrect diopter power.

Where Was This Sold?

Internationally to Vietnam.

About Tekia, Inc.

Tekia, Inc. has 2 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report