Z-1228-2020 Class II Terminated
FDA device recall Z-1228-2020 was initiated by CooperVision Inc. on January 13, 2020 and is designated Class II. Reason for recall: Incorrect power of lenses than the expected The recall status is terminated (terminated July 22, 2020). Affected quantity: 24.
Recall Details
- Product Type
- Devices
- Report Date
- February 19, 2020
- Initiation Date
- January 13, 2020
- Termination Date
- July 22, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 24
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
Distribution Pattern
US Nationwide Distribution
Code Information
Lot Numbers: 15628000006509 15628000007509