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 Model 872 Single Piece Hydrophilic Acrylic Intraocular Lenses Recalled by Tekia, Inc. Due to Mislabeling

Date: November 9, 2018
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 Model 872 Single Piece Hydrophilic Acrylic Intraocular Lenses, Diopter 15.0, Sterile. The firm name on the label is TEKIA, INC., Irvine, CA.

Quantity: 81 IOLs were distributed but only 36 within expiry were recalled

Why Was This Recalled?

A limited number of lenses may be mislabeled with the incorrect diopter power.

Where Was This Sold?

There was no U.S. distribution. Foreign distribution was made to Iran, Korea, Luxembourg, and 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