PlainRecalls
FDA Devices Moderate Class II Ongoing

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.

Reported: October 1, 2025 Initiated: August 22, 2025 #Z-2606-2025

Product Description

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.

Reason for Recall

One lot manufactured with an invalid sterilization cycle.

Details

Recalling Firm
CooperVision, Inc.
Units Affected
4,140 units
Distribution
US Nationwide distribution in the states of Florida, Kentucky, North Carolina, and Wisconsin.
Location
West Henrietta, NY

Frequently Asked Questions

What product was recalled?
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.. Recalled by CooperVision, Inc.. Units affected: 4,140 units.
Why was this product recalled?
One lot manufactured with an invalid sterilization cycle.
Which agency issued this recall?
This recall was issued by the FDA Devices on October 1, 2025. Severity: Moderate. Recall number: Z-2606-2025.