FDA recall record

Daytrana recall — FDA D-1249-2020

Defective Delivery System: Out of specification for mechanical peel and shear.

Class IIclassification
D-1249-2020official record ID
Apr 29, 2020report date

Recall record at a glance

Official recordD-1249-2020
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmNoven Therapeutics, LLC
Report dateApr 29, 2020
Recall initiation dateMar 31, 2020
Quantity14,142 30-count boxes
LocationMiami, FL, United States

Official product description

Daytrana (methylphenidate transdermal system) Delivers 30 mg over 9 hours (3.3 mg/hr) 30-count box, Rx only, Manufactured for Noven Therapeutics, LLC Miami, FL 33186, NDC 68968-5555-3

Why the product was recalled

Defective Delivery System: Out of specification for mechanical peel and shear.

Distribution information

Distributed Nationwide in the US

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.

DrugApr 29, 2020

Daytrana recall — FDA D-1247-2020

Defective Delivery System: Out of specification for mechanical peel and shear.

Class IIFDA: TerminatedNoven Therapeutics, LLC
DrugApr 29, 2020

Daytrana recall — FDA D-1248-2020

Defective Delivery System: Out of specification for mechanical peel and shear.

Class IIFDA: TerminatedNoven Therapeutics, LLC