FDAClass IIJanuary 14, 2015

HydrALAZINE Hydrochloride Tablets recall

HydrALAZINE Hydrochloride Tablets, USP 25 mg, 100 count bottle Rx only, Distributed by: Par Pharmaceutical Companies, Inc. Spring Valley, NY10977

Why was HydrALAZINE Hydrochloride Tablets recalled?

Presence of Foreign Substance: Par Pharmaceutical, Inc. is recalling one lot of HydrALAZINE Hydrochloride tablets due to the presence of small aluminum particles.

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 26708501, Exp. 01/17

Product
HydrALAZINE Hydrochloride Tablets, USP 25 mg, 100 count bottle Rx only, Distributed by: Par Pharmaceutical Companies, Inc. Spring Valley, NY10977
Recalling firm
Par Pharmaceutical Inc.
Quantity
38,788 bottles
Distribution
Nationwide
Recall date
January 14, 2015
Classification
Class II
Status
Terminated
Agency
FDA (drug)
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