Drug recall
Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours (1.1 mg/hr) Contains: 30 Patches, Rx…
FDA recall event 90162 · Class II · Noven Pharmaceuticals Inc
Key facts
| Event ID | 90162 |
|---|---|
| Recall numbers | D-0889-2022 |
| Recalling firm | Noven Pharmaceuticals Inc |
| Product type | Drugs |
| Products | Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours (1.1 mg/hr) Contains: 30 Patches, Rx only, Manufactured for Noven Therapeutics, LLC, Miami, FL 33186, By Noven… |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Defective Delivery System: customer complaints exceeded respective action limits. |
| Initiation date | May 6, 2022 |
| Report date | Jun 1, 2022 |
| City | Miami |
| State | FL |
| Country | United States |
| FEI number | 1000222037 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: