Z-1227-2020 Class II Terminated
FDA device recall Z-1227-2020 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: 216 units.
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
- 216 units
Product Description
Coopervision Vertex Toric /2 Clear Toric- Power -2.50 -0.75 /90 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: 15627000009010 15627050004010 16656000008010