CooperVision research shows that the FDA issued the recall this past October after hearing that CL wearers were experiencing hazy vision and discomfort. The CLs have also caused severe eye pain and eye injuries requiring medical treatment. The recall affects more than 600,000 lenses made between November 1 and August 3, 2011 which represents about 10 percent of all contact lenses sold throughout the United States.
According
to FDA reports, child wearers of the recalled toric CLs have experienced cornea injuries and other eye problems. According to the FDA, children have suffered corneal edema, corneal
abrasion and torn corneas. Children have also complained about
having the sensation of foreign-body, blurred vision, decrease in vision, eye pain or stinging/burning, light sensitivity,
redness of the eye, swollen eyelids, and increased tearing.
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