FDAMarch 17, 2017drug

LATANOPROST OPHTHALMIC SOLUTION, 0.005%, 125 ug/2.5 mL, packaged in 2.5 mL bottle, Rx only, Manufactured for: Akorn, Inc., Lake Forest, IL 60045, NDC 17478-625-12

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

The hazard

Lack of assurance of sterility: product was found to be empty, under-filled, or leaking.

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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