CooperVision recalls Pearle Vision 1 day contact lenses because some have the wrong power
A small number of Pearle Vision 1 day (somofilcon A) contact lenses in the affected lot are not the correct power.
What to do
The notice does not give instructions. Read the official notice for details.
Do not stop taking a prescribed medicine, or stop using a device you rely on, until you have talked to your pharmacist or doctor.
Recall details
- Product
- Brand Name: Pearle Vision 1 day Product Name: (somofilcon A) Contact Lens Model/Catalog Number: Pearle Vision 1 day
- Company
- CooperVision, Inc.
- Hazard
- A small number of lenses within the affected lot are of the incorrect power.
- Units
- 3060
- Where sold
- US Nationwide distribution in the states of MN, OH, WI.
- FDA classification
- Class II · Ongoing
- Classified by FDA
- September 18, 2026
- Recall started
- August 12, 2026
- FDA enforcement report
- September 30, 2026
- Identifiers
- Codes: Pearle Vision 1 day; Carton Lot # 11727620152030; Blister Lot # CB132348;
- FDA recall number: Z-3248-2026
The headline, summary and steps above are written in plain English from the official notice below. Identifiers are copied exactly as the agency published them. Always check the official notice before you act.
Official notice
The notice's own wording from FDA.
- 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.
- Classification
- Class II (Ongoing)
- Distribution
- US Nationwide distribution in the states of MN, OH, WI.
- Quantity
- 3060
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