Recall Z-0529-2015— Cooper Vision Caribbean Corp.
Class II · Terminated
Class II FDA medical device recall by Cooper Vision Caribbean Corp., initiated 2014-10-28, terminated 2015-10-02. FDA's recall record names no specific 510(k) clearance for this event. Product: Soft Contact Lens. Reason: Portions of the lots may contain units with an incorrect lens axis condition..
- Recalling firm
- Cooper Vision Caribbean Corp.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2014-10-28
- Terminated
- 2015-10-02
- Firm location
- Juana Diaz, PR, United States
Product description
Soft Contact Lens
Reason for recall
Portions of the lots may contain units with an incorrect lens axis condition.
Data sourced from openFDA. This site is unofficial and independent of the FDA.