March 2017 FDA Recall Drug by Akorn Inc
D-0696-2017 - Failed Dissolution Specifications

This Class II drug recall was voluntarily initiated by Akorn Inc on March 13, 2017 for the product Drug. The FDA reported the reason for recall as failed dissolution specifications. The product was distributed Nationwide and the recall is currently terminated.

Recall Number: D-0696-2017

Reason for Recall
Failed Dissolution Specifications
Initiated
03-13-2017
Reported
05-10-2017
Quantity
55,968 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
Sulfamethoxazole and Trimethoprim Oral Suspension, USP 200 mg / 40 mg per 5 mL , Grape Flavor, Rx Only, 16 fl oz. (473 mL), HI-TECH PHARMACAL CO., INIC, Amityville, NY 11701, NDC 50383-824-16

Batch or Lot Expiration Information

Lot# 348913, Exp.01/18
Lot# 349552, Exp.03/18
Lot# 349681, Exp. 03/18
Lot# 349683, Exp. 03/18
Lot# 349685, Exp. 03/18
Lot# 349687, Exp. 03/18
Lot# 349689, Exp. 03/18
Lot# 350636, Exp.03/18