Daytrana recalls
Daytrana products have been recalled 42 times, most recently on 29 Mar 2023. The recalling company is usually Noven Pharmaceuticals. The most common reason is potency & assay.
Total recalls42since 2012
Last 12 months0reported
Class I00% of total
Ongoing9latest 29 Mar 2023
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 42 100%Class III 0 0%
Why daytrana is recalled
Companies
Product types
By year
Ongoing daytrana recalls
9 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Daytrana (methylphenidate transdermal system) CII, 20mg recalledDaytrana | Noven Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Daytrana (methylphenidate transdermal system) CII, 15 mg recalledDaytrana | Noven Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Daytrana (methylphenidate transdermal system) CII, 10mg recalledDaytrana | Noven Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Daytrana (methylphenidate transdermal system) CII, 30 mg recalledDaytrana | Noven Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Daytrana (methylphenidate transdermal system) recalledDaytrana | Noven Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Daytrana (methylphenidate transdermal system) Delivers recalledDaytrana | Noven Pharmaceuticals | Other | Nationwide |
All daytrana recalls, newest first
42 totalAbout this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.