December 2019 FDA Recall Drug by Lannett Company, Inc.
D-0630-2020 - Microbial Contamination of Non-sterile Products

This Class I drug recall was voluntarily initiated by Lannett Company, Inc. on December 6, 2019 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-0630-2020

Reason for Recall
Microbial Contamination of Non-sterile Products: Out-of-specification results obtained for Total Aerobic Microbial Count.
Initiated
12-06-2019
Reported
12-25-2019
Quantity
16,668 bottles

Recall Profile & Regulatory Data

Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Lannett Company, Inc.
Nationwide within the United States
Levetiracetam Oral Solution 100mg/mL, 473 mL (16 fl. oz.) Bottles, Rx Only, Distributed by: Lannett Company, Inc. Philadelphia, PA 19136, NDC 54838-0548-80

Batch or Lot Expiration Information

Lot# : 2190A, 2191A, Exp. Date 07/2021