Medical device recalls Moderate risk

CooperVision, Inc. recalls Voyant 1-Day Premium Toric, (stenfilcon A) contact lens. Model Number: Voyant 1-Day Premium Toric. 54% water content, T…

Recall date
August 22, 2025
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-2608-2025
FDA classification
Class II
Brand / firm
CooperVision, Inc.
Sold / distributed
US Nationwide distribution in the states of Florida, Kentucky, North Carolina, and Wisconsin.

Why it was recalled

One lot manufactured with an invalid sterilization cycle.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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.

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