CLASS II Drug recall · Reported 15 Aug 2018 · FDA Enforcement Report

Valsartan/HCTZ 160/25mg Tablets recalled by NuCare Pharmaceuticals

NuCare Pharmaceuticals is recalling Valsartan/HCTZ 160/25mg Tablets, distributed in California. The recall was initiated on 30 Jul 2018 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot # T11443; Exp. 02/28/2019
Quantity recalledN/A

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-1038-2018
FDA event ID
80701
Recalling firm
NuCare Pharmaceuticals, Orange, CA
Classification
Class II
Status
Terminated
Recall initiated
30 Jul 2018
FDA classified
3 Aug 2018
Reported
15 Aug 2018
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Potency & Assay

Timeline

30 Jul 2018Recall initiated by company
3 Aug 2018Classified by FDA+4 days
15 Aug 2018Published 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: Carcinogen impurity detected in API used to manufacture drug product.

Potency and specification recalls happen when a batch tests outside its approved limits for strength, purity or dissolution, which can mean the dose delivered is higher or lower than labelled.

Product as listed by the FDA

Valsartan/HCTZ 160/25mg Tablets, 30-count jar, Rx Only, Packaged by NuCare Pharmaceuticals, Inc., Orange, CA 92867,

Where it was distributed

Distributed to three customers in Fl and CA

California

Questions about this recall

Is Valsartan/HCTZ 160/25mg Tablets recalled?

Yes. NuCare Pharmaceuticals recalled Valsartan/HCTZ 160/25mg Tablets on 30 Jul 2018. The recall is Class II and its status is Terminated. Recall number D-1038-2018.

Why was it recalled?

CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.

Which lots are affected?

Lot # T11443; Exp. 02/28/2019

Where was it sold?

Distributed to three customers in Fl and CA

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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