US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Jan 27, 2021 (6 years ago)

Spironolactone Tablets, USP, 50 mg, packaged in 30-count bottles, Rx only, Manufactured…

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

Why it was recalled

Labeling: Label Mix-Up - Prepackaged bottles labeled spironolactone 50 mg may contain spironolactone 25 mg tablets.

What was recalled

Spironolactone Tablets, USP, 50 mg, packaged in 30-count bottles, Rx only, Manufactured by: Frontida BioPharm, Inc., Philadelphia, PA 19124 USA, Repackaged by: Bryant Ranch Prepack, Inc., Burbank, CA 91504 USA, NDC 63629-1067-01

Recalling firm
Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals
NDC code
63629-1067-01
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0304-2021

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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