US Drug Recall Register
Class II · Moderate risk Terminated Initiated Mar 2, 2022 (5 years ago)

Alprazolam Tablets, USP 1mg, 180-count bottles, Rx only, Manufactured by ULTRAlab…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

CGMP Deviation: Potential cross-contamination with other drug substance during the manufacturing process.

What was recalled

Alprazolam Tablets, USP 1mg, 180-count bottles, Rx only, Manufactured by ULTRAlab Laboratories, Inc., NY; Packaged by GSMS, Inc., CA NDC 60429-504-18.

Recalling firm
Golden State Medical Supply Inc.
NDC code
60429-504-18
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0654-2022

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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