Medical Device Recall: Voyant 1-Day Premium Toric, (stenfilcon A) contact lens. Model Number: Voyant 1-Day Premium Toric. 54% water content, Toric, cast moulded Silicone Hydrogel, In-monomer tinted, contact lens, for Dai
CooperVision, Inc. · August 22, 2025
Reason for Recall
One lot manufactured with an invalid sterilization cycle.
Product Description
Voyant 1-Day Premium Toric, (stenfilcon A) contact lens. Model Number: Voyant 1-Day Premium 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
90 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2608-2025
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.