March 2017 FDA Recall Drug by Akorn, Inc.
D-0661-2017 - Lack of assurance of sterility

This Class II drug recall was voluntarily initiated by Akorn, Inc. on March 17, 2017 for the product Drug. The FDA reported the reason for recall as lack of assurance of sterility. The product was distributed Nationwide and the recall is currently terminated.

Recall Number: D-0661-2017

Reason for Recall
Lack of assurance of sterility: product was found to be empty, under-filled, or leaking.
Initiated
03-17-2017
Reported
04-19-2017
Quantity
107,940 bottles

Recall Profile & Regulatory Data

Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
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

Batch or Lot Expiration Information

Lot# LAB15G52, LAB11G52, Exp 6/17; LAB18I52, Exp 8/17; LAB9L52, 11/17; LAB1A62, LAB9A62, Exp 12/17