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US Oftalmi, in cooperation with the U.S. Food and Drug Administration (FDA), announced a nationwide recall of all over-the-counter eye drops and nasal drops.

The recall is being initiated due to conditions at the manufacturing facility that cannot assure sterility of the products.Non-sterile products have the potential to cause eye infections which can lead to serious eye sight problems.

No adverse effects, illness or injuries have been reported to date.

The recalled products were distributed nationwide to food and drug distributors. The FDA has a complete list of the recalled products which includes all affected lot numbers, expiration dates and UPC codes.

Consumers as well as healthcare professionals can report adverse events or side effects associated with this recall and others to the FDA’s MedWatch Safety Information Program online or by calling 1-800-332-1088

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