Recall Z-1228-2020— CooperVision Inc.
Class II · Terminated
Class II FDA medical device recall by CooperVision Inc., initiated 2020-01-13, terminated 2020-07-22. FDA's recall record names no specific 510(k) clearance for this event. Product: Coopervision Vertex Toric /2 Clear Toric- Power +2.25 -0.75/120 Soft (hydrophilic) Contact Lens (extended wear). Reason: Incorrect power of lenses than the expected.
- Recalling firm
- CooperVision Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2020-01-13
- Terminated
- 2020-07-22
- Firm location
- West Henrietta, NY, United States
Product description
Coopervision Vertex Toric /2 Clear Toric- Power +2.25 -0.75/120 Soft (hydrophilic) Contact Lens (extended wear)
Reason for recall
Incorrect power of lenses than the expected
Data sourced from openFDA. This site is unofficial and independent of the FDA.