Akorn, Inc. recalls LATANOPROST OPHTHALMIC SOLUTION, 0.005%, 125 ug/2.5 mL, packaged in 2.5 mL bottle, Rx only, Manufactured for: Akorn, I
Recalled April 19, 2017 · FDA recall D-0661-2017 · Akorn
Hazard
Lack of assurance of sterility: product was found to be empty, under-filled, or leaking. · FDA Class II
Units
107,940 bottles
Sold at
Nationwide
Description
Lack of assurance of sterility: product was found to be empty, under-filled, or leaking.
Product
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
Manufacturer(s)
Akorn, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →