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

Spironolactone tablets, USP 25 mg, Rx only, 500 count bottle, Distributed By: Greenstone…

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

Spironolactone tablets, USP 25 mg, Rx only, 500 count bottle, Distributed By: Greenstone LLC, Peapack, NJ 07977, NDC: 59762-5011-2.

Recalling firm
Greenstone Llc
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-010-2014

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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