CooperVision Vertex Toric Contact Lenses Recalled for Incorrect Power
CooperVision is recalling specific lots of Vertex Toric contact lenses because they were manufactured with an incorrect 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: The recall is classified as FDA Class II, but the source text does not report any hospitalizations, injuries, or illnesses. The hazard is a manufacturing defect (incorrect power) without reported adverse health consequences, fitting the criteria for a moderate severity score.
Plain-English summary
CooperVision Inc. is recalling 24 units of Vertex Toric /2 Clear Toric soft (hydrophilic) contact lenses (extended wear) with power +2.25 -0.75/120. The recall is due to the lenses having an incorrect power compared to the expected specification.
The affected products are identified by lot numbers 15628000006509 and 15628000007509. These lenses were distributed nationwide in the United States.
Consumers who possess these specific lot numbers should stop using the lenses and contact CooperVision Inc. for further instructions.
The recalled product
- Product
- Coopervision Vertex Toric /2 Clear Toric- Power +2.25 -0.75/120 Soft (hydrophilic) Contact Lens (extended wear)
- Manufacturer
- CooperVision Inc.
- Category
- Medical Device — Contact Lenses
- Hazard
- Affected units
- 24
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 Numbers: 15628000006509 15628000007509
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 2 recalled by CooperVision Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 2 products in this recall →Related recalls
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