CLASS II Drug recall · Reported 12 Mar 2014 · FDA Enforcement Report

Teva Hydroxyzine Pamoate Capsules, USP, 25 mg recalled

Teva Pharmaceuticals USA is recalling Teva Hydroxyzine Pamoate Capsules, USP, 25 mg, distributed nationwide in the US. The recall was initiated on 24 Jan 2014 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot # 34016752A, Exp. 09/16. Lot # 34016753A, Exp. 09/16.
NDC0555-0302, 0555-0323, 0555-0324
UPC0305550302025, 0305550323020
Quantity recalled35746 capsules

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-1095-2014
FDA event ID
67412
Recalling firm
Teva Pharmaceuticals USA, Horsham, PA
Manufacturer
Teva Pharmaceuticals USA, Inc.
Classification
Class II
Status
Terminated
Recall initiated
24 Jan 2014
FDA classified
28 Feb 2014
Reported
12 Mar 2014
Type
Voluntary: Firm initiated
Customers notified by
Letter

Timeline

24 Jan 2014Recall initiated by company
28 Feb 2014Classified by FDA+35 days
12 Mar 2014Published 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

CGMP Deviations: Hydroxyzine Pamoate Capsules, USP, 25 mg were manufactured using an unapproved material: API was incorrectly released for use in manufacturing.

Product as listed by the FDA

Teva Hydroxyzine Pamoate Capsules, USP, 25 mg, 100- count bottle, Rx Only,Distributed by Teva Pharmaceuticals, USA, Sellersville, PA. NDC 0555-0323-02.

Where it was distributed

Nationwide.

Nationwide

Questions about this recall

Why was it recalled?

CGMP Deviations: Hydroxyzine Pamoate Capsules, USP, 25 mg were manufactured using an unapproved material: API was incorrectly released for use in manufacturing.

Which lots are affected?

Lot # 34016752A, Exp. 09/16. Lot # 34016753A, Exp. 09/16.

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

Other products in this recall event

3 other products · FDA event 67412

This product is part of a recall event; the main page for the event is Teva Hydroxyzine Pamoate Capsules, USP, 100 mg recalled.

ReportedClassRecallCompanyReasonWhere
CLASS IITeva Hydroxyzine Pamoate Capsules, USP, 100 mg recalledHydroxyzine PamoateTeva Pharmaceuticals USAManufacturing (CGMP) DeviationsNationwide
CLASS IITeva Dextroamphetamine Saccharate, Amphetamine Asparate recalledDextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate And Amphetamine SulfateTeva Pharmaceuticals USAManufacturing (CGMP) DeviationsNationwide
CLASS IITeva Ethambutol Hydrochloride Tablets, USP, 400 mg recalledTeva Pharmaceuticals USAManufacturing (CGMP) DeviationsNationwide

More recalls from Teva Pharmaceuticals USA

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Other Hydroxyzine Pamoate recalls

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