US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jul 19, 2022 (4 years ago)

Prednisone Tablets USP, 20 mg, 100-count bottle, Rx Only, Manufactured by: Strides Pharma…

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

Why it was recalled

Presence of foreign tablet: 2.5 mg tablet in a 20 mg bottle of Prednisone Tablets

What was recalled

Prednisone Tablets USP, 20 mg, 100-count bottle, Rx Only, Manufactured by: Strides Pharma Science Ltd., Bengaluru - 562106, India, Distributed by: Strides Pharma Inc., East Brunswick, NJ 08816, NDC 64380-785-06.

Recalling firm
Strides Pharma Inc.
NDC code
64380-785-06
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1330-2022

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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