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Millions of Eye Drops Recalled Over Sterility Fears
3 Oct
Summary
- Hundreds of thousands of bottles of eye drops recalled due to potential lack of sterility.
- Sterling Pharmaceutical Services initiated the recall on August 20, 2026.
- FDA classified the recall as Class II, indicating temporary health risks.
A significant recall has been issued for hundreds of thousands of bottles of eye drops due to concerns about sterility. Sterling Pharmaceutical Services LLC initiated the recall on August 20, 2026. The U.S. Food and Drug Administration (FDA) subsequently classified the recall as Class II on September 21, 2026.
This recall encompasses nine different products, including lubricant eye drops, a hypertonicity solution, and a nighttime eye ointment. A total of 747,844 units are affected by this recall. The FDA's Class II classification indicates that exposure to the recalled product may cause temporary or medically reversible adverse health consequences, while the probability of serious adverse health consequences is considered remote.
Consumers are urged to verify if they possess any of the affected products. They should consult the FDA's recall information for specific lot numbers and expiration dates. If a product is part of the recall, it is advised to immediately discontinue its use and consult with a healthcare provider.
