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

Recall Number: D-0661-2017

Firm: Akorn, Inc.

Classification: Class II

Status: Terminated

Report Date: 20170419

Initiation Date: 20170317

Termination Date: 20190709

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

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