CooperVision Inc.: Medical Device Recall in 2018 - (Recall #: Z-1517-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

56% 1 Day Silicone Hydrogel (-4.50), 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.

Product Classification:

Class III

Date Initiated: February 21, 2018

Date Posted: May 2, 2018

Recall Number: Z-1517-2018

Event ID: 79755

Reason for Recall:

The secondary packaging is labeled with an incorrect expiration date.

Status: Terminated

Product Quantity: 328 packs/3280 lenses

Code Information:

Lot 14364100237018, Exp. Date 9/30/2020 (foil); 9/30/2022 (carton)

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated