Over-the-counter ophthalmic products were voluntarily recalled due to a manufacturing deviation discovered during a U.S. Food and Drug Administration audit, a notice says.

Nearly 76,000 cases of eye care products have been voluntarily recalled by their manufacturer following an audit by the U.S. Food and Drug Administration.

According to the recall notice, the exact health dangers for consumers using the recalled products are unknown, but the company said "deviations may lead to products of unacceptable quality, and it i...