US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jul 13, 2023 (3 years ago)

Methylphenidate Hydrochloride Tablets, USP 20mg, Rx Only, 100 Tablets per bottle…

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

Why it was recalled

Presence of Foreign Substance: Metal embedded in a tablet.

What was recalled

Methylphenidate Hydrochloride Tablets, USP 20mg, Rx Only, 100 Tablets per bottle, Manufactured by: Ohm Laboratories Inc., New Brunswick, NJ 08901, Distributed by: Sun Pharmaceutical Industries Inc., Cranbury, NJ 08512, NDC 57664-230-88.

Recalling firm
Sun Pharmaceutical Industries INC
NDC code
57664-230-88
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0940-2023

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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