40,000 bottles of eye drops across the US recalled over issues with sterility of product
Prestige Brand Holdings has voluntarily recalled nearly 40,000 bottles of Clear Eyes Maximum Itchy Eye Relief eye drops across the United States due to a lack of assurance of sterility. The Food and Drug Administration (FDA) classified this as a Class II recall, indicating a moderate risk of temporary or medically reversible adverse health consequences.

Briefing Summary
AI-generatedPrestige Brand Holdings has voluntarily recalled nearly 40,000 bottles of Clear Eyes Maximum Itchy Eye Relief eye drops across the United States due to a lack of assurance of sterility. The Food and Drug Administration (FDA) classified this as a Class II recall, indicating a moderate risk of temporary or medically reversible adverse health consequences. The recall specifically affects 15ml bottles with lot code 2552A and an expiration date of September 30, 2027. Consumers are advised to stop using the recalled product and return it for a refund. This recall follows a history of eye drop recalls, including a significant one in 2023 linked to bacterial contamination.
Article analysis
Model · rule-basedKey claims
4 extractedIn 2023, EzriCare Artificial Tears were recalled and linked to an outbreak of drug-resistant bacterial contamination, potentially causing one death and injuries to 68 people.
The recall specifically covers 15ml bottles with lot code 2552A and an expiration date of September 30, 2027.
The FDA classified the recall as a Class II recall, indicating a moderate-risk situation with potentially temporary or medically reversible adverse health consequences.
Nearly 40,000 bottles of Clear Eyes Maximum Itchy Eye Relief eye drops are being recalled across the US due to a lack of assurance of sterility.