US Drug Recall Register
Class III · Low risk Terminated Initiated Dec 18, 2017 (9 years ago)

Methylphenidate Hydrochloride Extended-release Tablets, USP 27 mg, 100-count bottles, Rx…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Subpotent Drug

What was recalled

Methylphenidate Hydrochloride Extended-release Tablets, USP 27 mg, 100-count bottles, Rx Only, Trigen Laboratories, LLC. Bridgewater, NJ 08807, NDC 13811-707-10

Recalling firm
Osmotica Pharmaceutical Corp
NDC code
13811-707-10
Origin
GA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0110-2018

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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