FDAClass IIJanuary 24, 2018

Divalproex Sodium Delayed Release Tablets USP recall: Contamination

Divalproex Sodium Delayed Release Tablets USP, 500 mg, 100-count bottle, RX Only, Manufactured by: Unichem Laboratories Ltd. Ind. Area, Meerut Road…

Why was Divalproex Sodium Delayed Release Tablets USP recalled?

Cross Contamination With Other Products: metronidazole powder was found in one bottle of Divalproex Sodium.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot: ZDPH17040

Product
Divalproex Sodium Delayed Release Tablets USP, 500 mg, 100-count bottle, RX Only, Manufactured by: Unichem Laboratories Ltd. Ind. Area, Meerut Road…
Recalling firm
Unichem Pharmaceuticals Usa Inc
Quantity
96,876 Bottles of 30s
Distribution
Product was distributed nationwide in the USA.
Recall date
January 24, 2018
Classification
Class II
Status
Terminated
Agency
FDA (drug)
Open FDA enforcement record Latest recalls