Class II

Medical Device Recall: 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. Bli

CooperVision, Inc. · August 22, 2025

Reason for Recall

One lot manufactured with an invalid sterilization cycle.

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.

Distribution

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

States Affected

NATIONWIDE

Quantity Affected

4,140 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2606-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

CooperVision, Inc. Medical Device Recall: 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. Bli | SafeCheck