FDA Initiates Recall of Millions of Rohto Eye Drop Products Over Sterility Issues

The FDA has issued a nationwide recall for approximately 11.96 million cartons of various Rohto Cooling Eye Drop products. This action stems from a lack of assurance regarding sterility during the manufacturing process, prompting a recommendation for consumers to cease using the affected items. This recall is significant due to the large volume of products involved and the potential health risks associated with non-sterile eye drops.