CLASS II Drug recall · Reported 25 Nov 2015 · FDA Enforcement Report

Hydrochlorothiazide Capsules, USP, 5 mg recalled

Vintage Pharmaceuticals LLC is recalling Hydrochlorothiazide Capsules, USP, 5 mg, distributed nationwide in the US. The recall was initiated on 7 Oct 2015 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesT084M14A, T085M14A, T086M14A; Exp 12/16
Quantity recalled912 HDPE bottles

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0232-2016
FDA event ID
72397
Recalling firm
Vintage Pharmaceuticals LLC, Huntsville, AL
Classification
Class II
Status
Terminated
Recall initiated
7 Oct 2015
FDA classified
13 Nov 2015
Reported
25 Nov 2015
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Particulate Matter

Timeline

7 Oct 2015Recall initiated by company
13 Nov 2015Classified by FDA+37 days
25 Nov 2015Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Presence of Particulate Matter.

Product as listed by the FDA

HYDROCHLOROTHIAZIDE CAPSULES, USP, 12.5 mg, 3000 count bottles, Rx only, Manufactured for: Qualitest Pharmaceuticals, Inc., Huntsville, AL 35811, NDC: 0603-3855-93.

Where it was distributed

Nationwide

Nationwide

Questions about this recall

Is Hydrochlorothiazide Capsules, USP, 5 mg recalled?

Yes. Vintage Pharmaceuticals LLC recalled Hydrochlorothiazide Capsules, USP, 5 mg on 7 Oct 2015. The recall is Class II and its status is Terminated. Recall number D-0232-2016.

Why was it recalled?

Presence of Particulate Matter.

Which lots are affected?

T084M14A, T085M14A, T086M14A; Exp 12/16

Where was it sold?

Nationwide

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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