Recall
FDAHealthAugust 22, 2025

CooperVision, Inc. — MyDay Toric, stenfilcon A) Contact Lens. Model/Catalog Number: MyDay Toric. 54% water content, Toric, cast moulded Silicone Hydrogel, In-monomer tinted, contact lens, for Daily

⚠️ One lot manufactured with an invalid sterilization cycle.

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
August 22, 2025

US Nationwide distribution in the states of Florida, Kentucky, North Carolina, and Wisconsin.

What's affected?

Product
MyDay Toric, stenfilcon A) Contact Lens. Model/Catalog Number: MyDay Toric. 54% water content, Toric, cast moulded Silicone Hydrogel, In-monomer tinted, contact lens, for Daily Disposable Wear. Blister packaged.
Lot code
20735504301008

Additional details

Carton Lot Number: 20735504301008. Blister Lot Number: 6450505898

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 4,140 units.

View original FDA notice →

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