Contact Lens Recall: CooperVision MyDay Toric
Announced 2025-10-01 · FDA
One lot of MyDay Toric contact lenses was manufactured with an invalid sterilization cycle. The recall involves 180 units distributed nationwide in the United States, including Florida, Kentucky, North Carolina, and Wisconsin. Identified affected lots are Carton Lot 20735504301008 and Blister Lot 6450505898.
| Brand | CooperVision, Inc. |
|---|---|
| Product | Sofmed Breathables, (stenfilcon A) contact lens. Model Number: Softmed Breathables. 54% water content, Toric, cast moulded Silicone Hydrogel, In-monomer tinted, contact lens, for Daily Disposable Wear. Blister packaged. |
| Reason | One lot manufactured with an invalid sterilization cycle. |
| Severity | moderate |
| Units affected | 4140 |
| Distribution | US Nationwide distribution in the states of Florida, Kentucky, North Carolina, and Wisconsin. |
| Agency | FDA |
WHAT YOU SHOULD DO
- Do not use lenses from the affected lots.
- Check the carton and blister lot numbers on your lenses; if they match 20735504301008 or 6450505898, stop wearing them and follow recall instructions for disposal or replacement.
- Contact CooperVision customer service or your eye care professional for guidance on disposal or replacement.
How to identify the recalled item
| Lot / date codes | Carton Lot Number: 20735504301008. Blister Lot Number: 6450505898 |
|---|---|
| Lot / date codes | Carton Lot Number: 20735504301008. Blister Lot Number: 6450505898 |
These are the identifiers FDA published for this recall. Most recall notices list no UPC or model number at all — if the code on your item is not shown here, that does not mean the item is excluded. Check the official notice, or contact the company.
Other contact lens recalls
- Contact Lens Recall: Pearle Vision 1 day · 2026-09-30
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.