The Recall Desk
ModerateFDA (Devices)·Z-1282-2023·Announced 2023-03-29

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.

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: 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
Hazard
  • manufacturing-defect
  • incorrect-power

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

Distributed nationwide across the United States.

Related recalls

Same category