FDAAugust 31, 2022drug

Sodium Chloride Ophthalmic Ointment USP, 5%, Sterile, Net Wt 3.5 g (1/8 oz) tube, Mfg by: Akorn, Inc., Lake Forest , IL 600405, NDC 17478-622-35

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

cGMP Deviations: Turbidity discovered in Artificial Tears Ointment during sterility testing. Scope expanded to include other lots and products which potentially share the same root cause.

What to do

FDA enforcement status: Terminated

Brands named

akorn

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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