FDA Issues Nationwide Recall for Eye Drops Due to Sterility Concerns
The Food and Drug Administration (FDA) has announced a nationwide recall of over 3 million eye drop containers, including those sold at San Antonio-area H-E-B stores. The recall, designated as a 'Class II recall,' was initiated on March 31 due to a 'lack of assurance of sterility.' This classification indicates that the adverse health consequences are either temporary or medically reversible, with a remote probability of serious health issues. The eye drop solutions, produced by K.C. Pharmaceuticals, Inc., a California-based company, were distributed under various brand names to major retailers such as H-E-B, Walgreens, Walmart, and CVS. The specific H-E-B-branded products affected include A.C. Eye Drops, Lubricant Eye Drops, and Original Eye Drops. Consumers are advised to check the FDA report for a complete list of product names, expiration dates, and specific stores involved. 
