CooperVision Recalls Pearle Vision 1 Day Contact Lenses Due to Incorrect Power
CooperVision is recalling specific lots of Pearle Vision 1 Day contact lenses because a small number of lenses have the incorrect power.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, but the hazard is incorrect lens power rather than a high-risk pathogen or structural defect, and no injuries are reported, fitting the Moderate criteria for low-risk contamination or labeling errors.
Plain-English summary
CooperVision, Inc. is recalling 3,060 units of Pearle Vision 1 Day (somofilcon A) contact lenses. The recall affects specific lots distributed in Minnesota, Ohio, and Wisconsin.
The recall was initiated because a small number of lenses within the affected lot are of the incorrect power. The affected products are identified by Carton Lot # 11727620152030 and Blister Lot # CB132348.
Consumers who have these specific lots of contact lenses should stop using them and contact their eye care professional or CooperVision for further instructions.
The recalled product
- Product
- Brand Name: Pearle Vision 1 day Product Name: (somofilcon A) Contact Lens Model/Catalog Number: Pearle Vision 1 day
- Manufacturer
- CooperVision, Inc.
- Category
- Medical Device — Contact Lenses
- Hazard
- Affected units
- 3,060
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (3)
- Pearle Vision 1 day
- Carton Lot # 11727620152030
- Blister Lot # CB132348
Distribution
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