FDAClass IIOctober 1, 2025

Voyant 1-Day Premium Toric recall

Voyant 1-Day Premium Toric, (stenfilcon A) contact lens. Model Number: Voyant 1-Day Premium Toric. 54% water content, Toric, cast moulded Silicone…

Why was Voyant 1-Day Premium Toric recalled?

One lot manufactured with an invalid sterilization cycle.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Carton Lot Number: 20735504301008. Blister Lot Number: 6450505898.

Product
Voyant 1-Day Premium Toric, (stenfilcon A) contact lens. Model Number: Voyant 1-Day Premium Toric. 54% water content, Toric, cast moulded Silicone…
Recalling firm
CooperVision, Inc.
Quantity
90 units
Distribution
US Nationwide distribution in the states of Florida, Kentucky, North Carolina, and Wisconsin.
Recall date
October 1, 2025
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls