Voyant 1-Day Toric Lens (CooperVision) – Sterilization Cycle (2025)
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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.
Brand
CooperVision, Inc.
Lot Codes / Batch Numbers
Carton Lot Number: 20735504301008. Blister Lot Number: 6450505898.
Products Sold
Carton Lot Number: 20735504301008. Blister Lot Number: 6450505898.
CooperVision, Inc. is recalling Voyant 1-Day Premium Toric, (stenfilcon A) contact lens. Model Number: Voyant 1-Day Premium Toric. due to One lot manufactured with an invalid sterilization cycle.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
One lot manufactured with an invalid sterilization cycle.
Recommended Action
Per FDA guidance
CooperVision contacted consignees via telephone call and letter on 08/27/2025. Consignees were instructed to examine inventory and quarantine affected lot numbers, cease further distribution of product, and notify customers/patients if further distributed. Consignees were also requested to complete and return the Correction Response Form and arrange for the return of affected units.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026