FDAFDA recall Z-3248-2026 · Sep 30, 2026
CooperVision, Inc.: Brand Name: Pearle Vision 1 day Product Name: (somofilcon A) Contact Lens Model/Catalog Nu recall
Recall found
Product
Brand Name: Pearle Vision 1 day Product Name: (somofilcon A) Contact Lens Model/Catalog Number: Pearle Vision 1 day
Reason for recall
A small number of lenses within the affected lot are of the incorrect power.
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your packaging. If this is a medicine or device you use, talk to your pharmacist or doctor before you stop or change anything, and contact the company or FDA for what to do with the product.
Recall details
- FDA classification
- Class II: use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
- Status
- Ongoing
- Codes, lots and dates
- Pearle Vision 1 day; Carton Lot # 11727620152030; Blister Lot # CB132348;
- Quantity
- 3060
- Distribution
- US Nationwide distribution in the states of MN, OH, WI.
- Recalling firm
- CooperVision, Inc., West Henrietta, NY
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-08-12
Source: openFDA enforcement record Z-3248-2026 · search recall number Z-3248-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 22, 2026, 4:56 AM EDT. The agency notice is the final word.