US Drug Recall Register
Class II · Moderate risk Terminated Initiated Sep 4, 2013 (13 years ago)

Aldactone (spironolactone) tablets, USP, 100 mg, 100-count bottles, Rx only, Distributed…

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

Why it was recalled

Marketed without an Approved NDA/ANDA: This recall is being initiated because of changes to the dissolution profile in distributed lots resulting from a manufacturing site change. There is currently no approved application supporting the alternate manufacturing site.

What was recalled

Aldactone (spironolactone) tablets, USP, 100 mg, 100-count bottles, Rx only, Distributed by G.D. Searle, Division of Pfizer Inc, NY, NY 10017, NDC 0025-1031-31

Recalling firm
Pfizer Us Pharmaceutical Group
NDC code
0025-1031-31
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-014-2014

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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