RecallRadar

FDA Device recall Z-1518-2018

56% 1 Day Silicone Hydrogel (-2.50), 10 pack, UV Blocking, daily disposable contact lenses The Clariti 1 Day (somofilcon A) Soft (Hydrophil…

On 2018-05-02 the FDA classified a Class III recall of 56% 1 Day Silicone Hydrogel (-2.50), 10 pack, UV Blocking, daily disposable contact lenses The Clariti 1 Day (somofilcon A) Soft (Hydrophil… by Coopervision, citing the secondary packaging is labeled with an incorrect expiration date.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1518-2018
ClassificationClass III
Statusterminated
Initiated2018-02-21
Published2018-05-02
Last updated2026-09-13 11:54 UTC
CompanyCoopervision
DistributionUS

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

The secondary packaging is labeled with an incorrect expiration date.

Identifiers

code_infoLot 14364100370010, Exp. Date 3/31/2020 (foil); 5/31/2020 (carton)

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1518-2018%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.