Voyant 1-Day Premium Toric Contact Lenses Recalled for Invalid Sterilization
CooperVision is recalling one lot of Voyant 1-Day Premium Toric contact lenses manufactured with an invalid sterilization cycle. Affected lenses are identified by carton lot 20735504301008 and blister lot 6450505898.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: This FDA Class II medical device recall involves contact lenses with an invalid sterilization cycle, creating a risk of microbial contamination and potential eye infections. Although no illnesses or injuries have been reported, improperly sterilized lenses pose a theoretical but significant risk to users, warranting a High severity classification.
Plain-English summary
CooperVision, Inc. is recalling one lot of Voyant 1-Day Premium Toric contact lenses because they were manufactured with an invalid sterilization cycle, which may result in improper sterilization of the product.
Contact lenses that are not properly sterilized may harbor microorganisms, potentially leading to eye infections or other complications when worn by consumers.
The recall affects 90 units distributed nationwide in Florida, Kentucky, North Carolina, and Wisconsin. The affected lot is identified by carton lot number 20735504301008 and blister lot number 6450505898.
Consumers who have purchased lenses from this lot should stop using them and contact their eye care professional for guidance on proper replacement options.
The recalled product
- 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.
- Manufacturer
- CooperVision, Inc.
- Category
- Medical Device — Contact Lenses
- Hazard
- sterilization-failure
- microbial-contamination-risk
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Carton Lot Number: 20735504301008. Blister Lot Number: 6450505898.
Distribution
Distributed nationwide across the United States.
Related recalls
Same category
- HighGE CARESCAPE Telemetry Server may lose patient ECG and oxygen saturation monitoring
FDA (Devices) · 2026-06-03
- HighGE APEXPRO and CARESCAPE Telemetry Systems Risk Loss of Patient Monitoring
FDA (Devices) · 2026-06-03
- SevereMedline Spinal Trays Recalled Due to Quality and Efficacy Concerns
FDA (Devices) · 2026-06-03
- HighPhilips Azurion and Allura Imaging Systems Recalled for Hard Drive Degradation
FDA (Devices) · 2026-06-03
- HighPhilips Allura Imaging Systems Hard Drive Degradation Affects Functionality
FDA (Devices) · 2026-06-03