Under pressure from the FDA, an Avaira contact lens recall was initiated by the manufacturer, CooperVision, in August 2011. After further investigation, CooperVision voluntarily expanded the recall later that year to include over 8 million lenses. The manufacturer and the FDA, however, stated only 600,000 actually made it to the public sector. Nonetheless, the side effects of the product have caused serious injury and permanent disability to a limited number of users.

Recently manufactured Sphere and Toric brands are not included in the Avaira contact lens recall. The manufacturer has developed higher quality assurance testing and formulas to protect consumer safety. CooperVision launched a website to assist consumers in checking if they own any of the tainted products. Alternatively, the company provided a toll-free hotline for consumers. However, the company notified consumers of the product, and instructed informed eye care specialists to get in touch with patients.

The Class I warning issued by the FDA is the strongest permitted indication of the seriousness of the adverse reactions. Users have been strongly urged to immediately remove the product and return it for a full refund. However, users that suffered serious adverse reactions that required medical attention may have just cause for a potential lawsuit.

High levels of silicone oil residue affected the brands Toric and Sphere resulting in injury ranging from mild eye initiation to severe eye pain. The lubricant, while safe for the eyes in low doses, is an irritant at high levels that may cause damage. The side effects include:
– Torn corneas
– Blurry or hazy vision
– Corneal abrasion
– Reduced vision
– Agonizing eye pain
– Blindness

Wearers would immediately notice eye irritation upon placement of the product. If the product was removed quickly, the side effects would cease in under 30-minutes. However, there have been reports of serious reactions to the silicone oil residue that required immediate medical attention. Sufferers reported severely debilitating pain and altered vision that was serious enough to require surgery. To date, no deaths have been reported.

The Avaira contact lens recall was voluntary after consumer complaints of eye injury. Blindness lasting for up to 12-weeks has been noted, but the condition is temporary. However, the loss of sight causes discomfort, lost wages, and suffering. Other users suffered immediate excruciating pain that requires emergency room visits and medical treatment. Every user experiences different symptoms and adverse effects, and the company has made the safety and health of customers its top priority.

For the user that currently has the product associated with the Avaira contact lens recall at home, it is important to not use the product. Return the product to the eye care specialist for a full refund or replacement. If there is any discomfort, get a hold of a qualified medical professional. While the side effects may cease after removal of the product, in some cases, the pain continues. If there has been serious injury contact a qualified attorney immediately.

Consumers have legal recourse, especially when medical attention is necessary. The company is held responsible for providing the consumer with a tainted product. The attorney can verify that the product is part of the Avaira contact lens recall. Contacting a qualified attorney that is trained with personal injury law may provide both financial compensation and peace of mind.