Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

Zenlens Toric-Gas Permeable Contact lenses for Daily Wear in a Recalled by Alden Optical Due to Vials labeled for the prescriptions contained incorrect lenses

Date: July 3, 2018
Company: Alden Optical
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 Alden Optical directly.

Affected Products

Zenlens Toric-Gas Permeable Contact lenses for Daily Wear in a 10-cc polycarbonate vial (Rx) as follows: Zenlens FT(Front Toric); Zenlens Toric-Zenlens FT + MV (Front Toric+Microvault); Zenlens TPC-(Toric Peripheral Curve); Zenlens TPC + FT- (Toric Peripheral Curve + FrontToric) Zenlens TPC + MV- (Toric Peripheral Curve+Microvault). Catalog Number: AOZNT Zenlens Toric - Zenlens contact lenses are indicated for daily wear for the correction of refractive arnetropia (myopia, hyperopia, and astigmatism) in aphakic and nonaphakic persons with non-diseased eyes.

Quantity: 36 vials

Why Was This Recalled?

Vials labeled for the prescriptions contained incorrect lenses

Where Was This Sold?

This product was distributed to 13 states: CA, GA, IL, MD, NV, NJ, NC, OH, OK, PA, TN, TX, UT

Affected (13 states)Not affected

About Alden Optical

Alden Optical has 13 total recalls tracked by RecallDetector.

Related Recalls

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