CLASS II Drug recall · Reported 12 Apr 2023 · FDA Enforcement Report

Alprazolam Tab, USP 0.25mg, (CIV) recalled by Preferred Pharmaceuticals

Preferred Pharmaceuticals is recalling Alprazolam Tab, USP 0.25mg, (CIV), distributed nationwide in the US. The recall was initiated on 27 Mar 2023 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot: G1822K, Exp. Date:5/31/2023.
Quantity recalled30 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-0504-2023
FDA event ID
92008
Recalling firm
Preferred Pharmaceuticals, Anaheim, CA
Classification
Class II
Status
Terminated
Recall initiated
27 Mar 2023
FDA classified
5 Apr 2023
Reported
12 Apr 2023
Type
Voluntary: Firm initiated
Customers notified by
Letter

Timeline

27 Mar 2023Recall initiated by company
5 Apr 2023Classified by FDA+9 days
12 Apr 2023Published in enforcement report+7 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: Downstream recall from Breckenridge Pharmaceuticals, Inc due to potential risk of Cross Contamination.

Product as listed by the FDA

Alprazolam Tab, USP 0.25mg, (CIV), 30-count bottle, Rx Only, Preferred Pharmaceuticals, Inc. Manufactured by: Breckenridge Pharmaceuticals, Inc., Boca Raton, FL. Ins:NDC 68788-7594-3

Where it was distributed

Nationwide in the USA

Nationwide

Questions about this recall

Why was it recalled?

CGMP Deviations: Downstream recall from Breckenridge Pharmaceuticals, Inc due to potential risk of Cross Contamination.

Which lots are affected?

Lot: G1822K, Exp. Date:5/31/2023.

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 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

2 other products · FDA event 92008

More recalls from Preferred Pharmaceuticals

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Other Alprazolam Tab recalls

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