CooperVision recall: (somofilcon A) Contact Lens
CooperVision, Inc. is recalling (somofilcon A) Contact Lens – 3060. The U.S. Food and Drug Administration published the recall on September 30, 2026; it began on August 12, 2026. Distributed nationwide.
Serious Class II means the product may cause temporary or medically reversible health problems, or the chance of serious harm is remote.
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| Product | (somofilcon A) Contact Lens |
| Brand | CooperVision |
| Company | CooperVision, Inc. |
| Type | Medical devices |
| Classification | Class II |
| Recall date | August 12, 2026 |
| Published by FDA | September 30, 2026 |
| Quantity | 3060 |
| Recall ID | 99766 |
Recalled products
- Brand Name: Pearle Vision 1 day Product Name: (somofilcon A) Contact Lens Model/Catalog Number: Pearle Vision 1 day
- FDA recall number
- Z-3248-2026
- Codes, lots and dates
- Pearle Vision 1 day; Carton Lot # 11727620152030; Blister Lot # CB132348;
- Quantity
- 3060
- Classification
- Class II
Identifiers and details
- FDA event ID
- 99766
- Initiated
- Voluntary: Firm initiated
- Status
- Ongoing
- Firm location
- West Henrietta, NY, United States
Why it was recalled
The reason the FDA lists: “A small number of lenses within the affected lot are of the incorrect power.”
Where it was sold
Nationwide. Distribution as the FDA records it: “US Nationwide distribution in the states of MN, OH, WI.”
What to do
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Official notice: FDA Enforcement Report record (event 99766, openFDA) – the same recall numbers can be searched in the FDA Enforcement Report.
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About this recall
Is CooperVision (somofilcon A) Contact Lens recalled?
Yes. CooperVision, Inc. recalled it on August 12, 2026; FDA published it September 30, 2026 (Class II). Only the lots, dates or models listed on this page are included.
Why was it recalled?
A small number of lenses within the affected lot are of the incorrect power.
What should I do if I have it?
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Where was it sold?
Nationwide.
More recalls
Source: recall records published by the U.S. Food and Drug Administration (openFDA Enforcement Reports), the USDA Food Safety and Inspection Service, the Consumer Product Safety Commission and the National Highway Traffic Safety Administration, collected twice a day. Product names, lot codes, dates and model numbers are shown exactly as the agency lists them; the agency's notice is the authority. 77.today is not affiliated with any of these agencies.