US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jun 17, 2024 (2 years ago)

Methylphenidate Hydrochloride, Extended-release Tablets, USP, 36mg, 100-count Bottle, Rx…

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

Why it was recalled

Failed dissolution specifications: this product is being recalled due to this batch not meeting dissolution specifications.

What was recalled

Methylphenidate Hydrochloride, Extended-release Tablets, USP, 36mg, 100-count Bottle, Rx Only, Manufactured for: Trigen Laboratories, LLC, Alpharetta, GA 30005, NDC 13811-708-10

Recalling firm
Trigen Laboratories
NDC code
13811-708-10
Origin
GA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0579-2024

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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