CLASS II Drug recall · Reported 9 Mar 2022 · FDA Enforcement Report

Alprazolam Tablets, USP 1mg, Generic for Xanax, Pkg Size: a) recalled

Preferred Pharmaceuticals is recalling Alprazolam Tablets, USP 1mg, Generic for Xanax, Pkg Size: a) per, distributed nationwide in the US. The recall was initiated on 22 Feb 2022 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #s: a) G2919M, I0619O, F1419J; b) H3019Q; c) F1219N, F1919D, H0219D, I0519R, J0319G, Exp. 03/31/2022.
Quantity recalled276 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-0642-2022
FDA event ID
89656
Recalling firm
Preferred Pharmaceuticals, Anaheim, CA
Classification
Class II
Status
Terminated
Recall initiated
22 Feb 2022
FDA classified
1 Mar 2022
Reported
9 Mar 2022
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Timeline

22 Feb 2022Recall initiated by company
1 Mar 2022Classified by FDA+7 days
9 Mar 2022Published in enforcement report+8 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

Product as listed by the FDA

Alprazolam Tablets, USP 1mg, Generic for Xanax, Pkg Size: a) 30 tablets per bottle, NDC: 68788-6381-03, b) 60 tablets per bottle, NDC: 68788-6381-06, c) 90 tablets per bottle, NDC: 68788-6381-09, Mfg: Par Pharmaceutical.

Where it was distributed

Nationwide in the USA.

Nationwide

Questions about this recall

Is Alprazolam Tablets, USP 1mg, Generic for Xanax, Pkg Size: a) per recalled?

Yes. Preferred Pharmaceuticals recalled Alprazolam Tablets, USP 1mg, Generic for Xanax, Pkg Size: a) per on 22 Feb 2022. The recall is Class II and its status is Terminated. Recall number D-0642-2022.

Why was it recalled?

CGMP deviations

Which lots are affected?

Lot #s: a) G2919M, I0619O, F1419J; b) H3019Q; c) F1219N, F1919D, H0219D, I0519R, J0319G, Exp. 03/31/2022.

Where was it sold?

Nationwide in the USA.

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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