US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Aug 5, 2025 (13 months ago)

Spironolactone Tablets, USP, 25 mg, 100-count bottle, Rx only, Mfg. by: Frontida…

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

Why it was recalled

Presence of foreign substance: identified as aluminum.

What was recalled

Spironolactone Tablets, USP, 25 mg, 100-count bottle, Rx only, Mfg. by: Frontida BioPharm, Inc., 1100 Orthodox St, Philadelphia, PA 19124, Dist. by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, NDC 53489-143-01

Recalling firm
Sun Pharmaceutical Industries INC
NDC code
53489-143-01
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0574-2025

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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