# FDA recall Z-2981-2018

> **Alden Optical** · Class III · device recall initiated 2018-07-03.

## Product

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.

## Reason for recall

Vials labeled for the prescriptions contained incorrect lenses

## Distribution

US Distribution in the states of: CA, GA, IL, MD, NC, NJ, NV, OH, OK,  PA, TN, TX and UT.

## Key facts

- **Recall number:** Z-2981-2018
- **Recalling firm:** Alden Optical
- **Classification:** Class III
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-07-03
- **Report date:** 2018-09-12
- **Termination date:** 2020-02-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Lancaster, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2981-2018

## Citation

> AI Analytics. FDA recall Z-2981-2018. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-2981-2018. Source: US FDA. Licensed CC0.

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