Safety Alerts & Recalls

Alerts for Methylphenidate

Title Date Published Source
Arzneimittelkommission warnt vor möglichem Leberversagen durch Methylphenidat 2015-02-17
FDA Raises Concern About Generic Extended-Release Methylphenidate Hydrochloride Tablets (generic Concerta) made by Mallinckrodt and Kudco 2014-11-14
FDA Warns of Rare Risk of Priapism Associated with Methylphenidate Products 2013-12-17
Les laboratoires NOVARTIS, JANSSEN et SHIRE rappellent aux professionnels de santé l’utilisation appropriée des traitements à base de méthylphénidate 2012-10-15
Noven Pharmaceutical Recalls One More Lot of Daytrana Patches 2012-07-25
Noven Pharmaceutical Recalls Several Lots of Daytrana Patches 2012-07-22
Mallinckrodt Inc. Recalls Several Lots of Methylin Chewable Tablets (methylphenidate HCl) 2.5 mg, 5 mg and 10 mg 2012-07-20
Noven Pharmaceuticals, Inc Recalls Several Lots of Daytrana (methylphenidate) Patch, 20 mg and 30 mg 2012-03-19
FDA Issues Safety Review Update of Medications Used to Treat Attention-Deficit/Hyperactivity Disorder (ADHD) 2011-11-02
Non-Safety-Related Recall of Several Lots of Daytrana Patches 2011-07-21
Delay in Results From FDA's Ongoing Safety Review of Stimulant Medications used in Children with ADHD 2010-08-05
Additional List of Recalled Lots of Daytrana Patches Published By FDA 2010-06-11
Non-Safety-Related Recall of a Limited Portion of Daytrana Patches 2010-04-02
MHRA Review of METHYLPHENIDATE and Risk of Genetic Damage and Update to Patient Information Leaflet 2010-02-15
Ongoing FDA Safety Review of Stimulant Mediations Used to Treat ADHD in Children 2009-06-16
Several lots of DAYTRANA (methylphenidate transdermal system) Voluntarily Recalled 2009-03-20
Risk of Burns during MRI Scans from Transdermal Drug Patches with Metallic Backings 2009-03-09
Several lots of DAYTRANA (methylphenidate transdermal system) voluntarily recalled 2008-08-26
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