Safety Alert: Class II: One lot manufactured with an invalid sterilization cycle.
healthClass IIRecalled on Oct 1, 2025
MyDay Toric, stenfilcon A) Contact Lens. Model/Catalog Number: MyDay Toric. 54% water content, Toric, cast moulded Silicone Hydrogel
🔢 4,140 units
Sold At: CooperVision, Inc.(US Nationwide distribution in the states of Florida, Kentucky, North Carolina, and Wisconsin.)
Recall #: FDA-DEVICE-Z-2606-2025
Source: FDA-ENFORCEMENT
Product Identification
- Lot/Batch Codes:
- Carton Lot Number: 20735504301008. Blister Lot Number: 6450505898
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Summary
One lot manufactured with an invalid sterilization cycle.
What to do next
- 1Stop using this product - may cause temporary or medically reversible health problems
- 2Check with retailer or manufacturer for recall status and remedy options
- 3Contact CooperVision, Inc. for return or refund information
- 4Visit the official FDA recall page for complete details
Summaries only; always follow the official notice.