CooperVision Vertex Toric Contact Lenses Recalled for Incorrect Power
CooperVision is recalling 216 units of Vertex Toric contact lenses because they have an incorrect power than expected.
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. The hazard is incorrect lens power, which is a labeling/specification error rather than a contamination or structural defect causing immediate physical injury. No injuries or illnesses are reported in the source text.
Plain-English summary
CooperVision Inc. is recalling 216 units of Vertex Toric soft (hydrophilic) contact lenses. The recall is due to the lenses having an incorrect power than the expected power.
The affected product is the Vertex Toric /2 Clear Toric- Power -2.50 -0.75 /90 Soft (hydrophilic) Contact Lens (extended wear). The recall involves specific lot numbers: 15627000009010, 15627050004010, and 16656000008010. The product was distributed nationwide in the US.
Consumers who have these specific contact lenses should stop using them and contact their eye care professional or CooperVision for further instructions.
The recalled product
- Product
- Coopervision Vertex Toric /2 Clear Toric- Power -2.50 -0.75 /90 Soft (hydrophilic) Contact Lens (extended wear)
- Manufacturer
- CooperVision Inc.
- Category
- Medical Device — Contact Lenses
- Hazard
- Affected units
- 216
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: 15627000009010 15627050004010 16656000008010
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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