The manufacturer of 27 different eyedrop products has issued a voluntary recall after the U.S. Food and Drug Administration said the eyedrops should not be used because inspectors found unsanitary conditions at the manufacturing plant in India.
The United States Federal Drug Administration (FDA) has enlarged the list of eye drops recalled in 2023 due to the possibility of bacterial contamination
The manufacturer of 27 different eyedrop products has issued a voluntary recall. U.S. Food and Drug Administration said inspectors found unsanitary conditions at the manufacturing plant in India.