Methylphenidate Hydrochloride: 10 recalls on record

Recalled by 1 agency: FDA (10).

First recall on record: August 14, 2013. Most recent: July 10, 2024.

Risk classification: Class II: 8 · Class III: 2

Most recent recalls

DateAgencyProduct
July 10, 2024FDAMethylphenidate Hydrochloride, Extended-release Tablets, USP, 36mg, 100-count Bottle, Rx …D-0579-2024
August 2, 2023FDAMethylphenidate Hydrochloride Tablets, USP 20mg, Rx Only, 100 Tablets per bottle, Manufac…D-0940-2023
March 2, 2022FDAMethylphenidate Hydrochloride Chewable Tablets, 2.5 mg, 100-count bottle, Rx Only, Manufa…D-0573-2022
February 19, 2020FDAMethylphenidate hydrochloride Extended-Release ablets USP (CII), 27 mg, 100-count bottle,…D-0837-2020
February 19, 2020FDAMethylphenidate hydrochloride Extended-Release ablets USP (CII), 18 mg, 100-count bottle,…D-0836-2020
December 27, 2017FDAMethylphenidate Hydrochloride Extended-release Tablets, USP 27 mg, 100-count bottles, Rx…D-0110-2018
December 27, 2017FDAMethylphenidate Hydrochloride Extended-release Tablets, USP 54 mg, 100-count bottles, Rx …D-0111-2018
August 14, 2013FDAMethylphenidate Hydrochloride Extended-Release Capsules (LA), 20 mg, 100 count bottle, Rx…D-847-2013
August 14, 2013FDAMethylphenidate Hydrochloride Extended-Release Capsules (LA), 40 mg, 100 count bottle, Rx…D-849-2013
August 14, 2013FDAMethylphenidate Hydrochloride Extended-Release Capsules (LA), 30 mg, 100 count bottle, Rx…D-848-2013

Questions about this brand

How many recalls does Methylphenidate Hydrochloride have?
Recalert has 10 U.S. recalls on record for Methylphenidate Hydrochloride, published between August 14, 2013 and July 10, 2024.
What was the most recent Methylphenidate Hydrochloride recall?
FDA recall D-0579-2024, published July 10, 2024: Methylphenidate Hydrochloride, Extended-release Tablets, USP, 36mg, 100-count Bottle, Rx Only, Manufactured for: Trigen Laboratories, LLC, Alpharetta, GA 30005, NDC 13811-708-10
Which agencies have recalled Methylphenidate Hydrochloride products?
Methylphenidate Hydrochloride products appear in recalls from: FDA (10).

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