December 2017 FDA Recall Divalproex Sodium by Unichem Pharmaceuticals Usa Inc
D-0228-2018 - Cross Contamination With Other Products

This Class II drug recall was voluntarily initiated by Unichem Pharmaceuticals Usa Inc on December 19, 2017 for the product Divalproex Sodium. The FDA reported the reason for recall as cross contamination with other products. The product was distributed Nationwide and the recall is currently terminated.

Recall Number: D-0228-2018

Reason for Recall
Cross Contamination With Other Products: metronidazole powder was found in one bottle of Divalproex Sodium.
Initiated
12-19-2017
Reported
01-24-2018
Quantity
96,876 Bottles of 30s

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
Unichem Pharmaceuticals Usa Inc
Product was distributed nationwide in the USA.
Divalproex Sodium Delayed Release Tablets USP, 500 mg, 100-count bottle, RX Only, Manufactured by: Unichem Laboratories Ltd. Ind. Area, Meerut Road, Ghaziabad-201 003, India. Marketed By: Unichem Pharmaceuticals (USA), Inc. Hasbrouck Heights, NJ 07604. NDC 29300-140-01

Batch or Lot Expiration Information

Lot# Lot: ZDPH17040