FDA recall record

CooperVision clariti 1 day (-1.25) 90 pack, UV Blocking, 90 silicone hydrogel, daily recall — FDA Z-1516-2018

The secondary packaging is labeled with an incorrect expiration date.

Class IIIclassification
Z-1516-2018official record ID
May 2, 2018report date

Recall record at a glance

Official recordZ-1516-2018
CategoryMedical Device Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmCooperVision Inc.
Report dateMay 2, 2018
Recall initiation dateFeb 21, 2018
Quantity32 packs/2880 lenses
LocationW Henrietta, NY, United States

Official product description

clariti 1 day (-1.25) 90 pack, UV Blocking, 90 silicone hydrogel, 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.

Why the product was recalled

The secondary packaging is labeled with an incorrect expiration date.

Distribution information

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.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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