January 2015 FDA Recall Drug by Akorn, Inc.
D-0385-2015 - Microbial Contamination of Non-Sterile Products

This Class II drug recall was voluntarily initiated by Akorn, Inc. on January 28, 2015 for the product Drug. The FDA reported the reason for recall as microbial contamination of non-sterile products. The product was distributed Nationwide and the recall is currently terminated.

Recall Number: D-0385-2015

Reason for Recall
Microbial Contamination of Non-Sterile Products: Active Pharmaceutical Ingredient (API) failed USP microbial tests.
Initiated
01-28-2015
Reported
02-18-2015
Quantity
23,449 jars

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
Erythromycin Pledgets USP, 2%, 60-count jar,Rx only, Manufactured by Ei LLC, Kannapolis, NC 28083, Marketed by VersaPharm Incorporated, Marietta, GA 30062, NDC 61748-202-60 .

Batch or Lot Expiration Information

Lot# 1446800; Exp. 03/15
Lot# 1538100; Exp. 05/15
Lot# 1538101; Exp. 05/15
Lot# 1538200; Exp. 06/15
Lot# 1608200; Exp. 08/15