Contact Lens Recall: CooperVision Clariti 1-day Toric With Incorrect Power
CooperVision is recalling Clariti 1-day toric contact lenses from lot W0124677 because they were made with a misaligned axis that results in incorrect lens power.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
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: This is an FDA Class II recall for a manufacturing defect affecting vision correction function. No illnesses or injuries have been reported. The hazard is functional rather than an immediate health or safety risk.
Plain-English summary
CooperVision, Inc. is recalling Clariti 1-day toric soft contact lenses with power -1.00 -1.25/90 from lot number W0124677. Approximately 3,150 units are affected.
The lenses were manufactured with a misaligned axis that results in incorrect optical power. This means the lenses do not provide the intended vision correction.
These lenses were distributed nationwide in the United States in Florida, Illinois, New York, Utah, and Wisconsin, as well as in Canada.
Patients with these lenses should stop using them and contact their eye care provider for replacement.
The recalled product
- Product
- Clariti 1-day toric soft contact lenses, Power -1.00 -1.25/90
- Manufacturer
- CooperVision, Inc.
- Category
- Medical Device — Contact Lenses
- Affected units
- 3,150
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 (1)
- Lot Number W0124677
Distribution
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Similar recalls
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