CooperVision MyDay Toric Contact Lenses: Invalid Sterilization Cycle Risk
CooperVision recalls MyDay Toric contact lenses made with an invalid sterilization cycle. This could lead to improper lens safety. Affected units include specific lot numbers from 20735504301008 carton.
Recall notice
One lot manufactured with an invalid sterilization cycle.
Contact the company
What happened, in plain English
CooperVision is recalling MyDay Toric contact lenses that were manufactured with an invalid sterilization cycle. This could mean the lenses are not properly sterilized, posing a risk of infection or injury if used. Read more at govinfonow.com/recall/51549-coopervision-myday-toric-contact-lenses-invalid-sterilization-cycle-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/51549-coopervision-myday-toric-contact-lenses-invalid-sterilization-cycle-risk · Updated August 17, 2026 · FDA enforcement record: FDA #Z-2606-2025
Cite this page
“CooperVision MyDay Toric Contact Lenses: Invalid Sterilization Cycle Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/51549-coopervision-myday-toric-contact-lenses-invalid-sterilization-cycle-risk. Based on FDA recall #Z-2606-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2606-2025%22&limit=1).
Why it’s dangerous
The lenses were made using an invalid sterilization cycle, which means they may not be properly cleaned or disinfected. This could lead to bacterial growth or other contaminants on the lenses, increasing the risk of eye infections or injury.
Who’s affected
Contact lens wearers who purchased the MyDay Toric lenses with carton lot number 20735504301008 are affected. People who use these lenses daily are at higher risk due to potential contamination.
How to tell if you have this one
Check for carton lot number 20735504301008 on the packaging. The product is a daily disposable contact lens with 54% water content, toric design, and stenfilcon A material.
- Brand
CooperVision- Category
Medical device
All 3 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Ongoing- Distribution
US Nationwide distribution in the states of Florida, Kentucky, North Carolina, and Wisconsin.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| Z-2606-2025 | MyDay Toric, stenfilcon A) Contact Lens. Model/Catalog Number: MyDay Toric. 54% water content, Toric, cast moulded Silicone Hydrogel, In-monomer tinted, contact lens, for Daily Disposable Wear. Blister packaged.; Carton Lot Number: 20735504301008. Blister Lot Number: 6450505898 | 4,140 units |
| Z-2607-2025 | 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.; Carton Lot Number: 20735504301008. Blister Lot Number: 6450505898 | 180 units |
| Z-2608-2025 | 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.; Carton Lot Number: 20735504301008. Blister Lot Number: 6450505898. | 90 units |
What to do — step by step
Check Packaging
Look for carton lot number 20735504301008 on the blister pack or carton.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 4 states.
FDA distribution: “US Nationwide distribution in the states of Florida, Kentucky, North Carolina, and Wisconsin.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Florida, Kentucky, North Carolina, Wisconsin.
Recall timeline
FDA published this recall 40 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-2606-2025 (August 22, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2606-2025 to see it in context.
- Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.