# FDA recall Z-1518-2018

> **CooperVision Inc.** · Class III · device recall initiated 2018-02-21.

## Product

56% 1 Day Silicone Hydrogel  (-2.50), 10 pack, UV Blocking, daily disposable contact lenses     The Clariti 1 Day (somofilcon A) Soft (Hydrophilic) Daily Disposable Contact Lens with UV blocker is indicated for daily wear single use only for the correction of refractiveametropia (myopia and hyperopia) in phakic or aphakic persons with non-diseased eyes that may exhibit astigmatism up to 2.00 Dopters that does not interfere with visualacuity. Clariti 1 Day (somofilcon A) Soft (Hydrophilic) Daily Disposable Contact Lens with UVblocker help protect against transmission of harmful UV radiation to the cornea andinto the eye.

## Reason for recall

The secondary packaging is labeled with an incorrect expiration date.

## Distribution

US Nationwide Distribution to states of: AL, AR, CA, CO, FL, GA, HI, IA, IL, IN, KS, KY, MD, ME, MI, MN, MO, MS, NC, NE, NH, NJ, NY, OH, OR, PA, SC, TN, TX, UT, VA, WA, WI, and WY.

## Key facts

- **Recall number:** Z-1518-2018
- **Recalling firm:** CooperVision Inc.
- **Classification:** Class III
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-02-21
- **Report date:** 2018-05-02
- **Termination date:** 2019-10-02

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1518-2018

## Citation

> AI Analytics. FDA recall Z-1518-2018. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-1518-2018. Source: US FDA. Licensed CC0.

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