FDAClass IINovember 25, 2015

Hydrochlorothiazide Capsules recall: Particulate Matter

HYDROCHLOROTHIAZIDE CAPSULES, USP, 12.5 mg, 3000 count bottles, Rx only, Manufactured for: Qualitest Pharmaceuticals, Inc., Huntsville, AL 35811, NDC…

Why was Hydrochlorothiazide Capsules recalled?

Presence of Particulate Matter.

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?

T084M14A, T085M14A, T086M14A; Exp 12/16

Product
HYDROCHLOROTHIAZIDE CAPSULES, USP, 12.5 mg, 3000 count bottles, Rx only, Manufactured for: Qualitest Pharmaceuticals, Inc., Huntsville, AL 35811, NDC…
Recalling firm
Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals
Quantity
912 HDPE bottles
Distribution
Nationwide
Recall date
November 25, 2015
Classification
Class II
Status
Terminated
Agency
FDA (drug)
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