# FDA recall D-0889-2022

> **Noven Pharmaceuticals Inc** · Class II · drug recall initiated 2022-05-06.

## Product

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 Pharmaceuticals, Inc., Miami, FL, 33186, NDC 68968-5552-3

## Reason for recall

Defective Delivery System: customer complaints exceeded respective action limits.

## Distribution

Nationwide to the U.S. Market

## Key facts

- **Recall number:** D-0889-2022
- **Recalling firm:** Noven Pharmaceuticals Inc
- **Classification:** Class II
- **Product type:** drug
- **Status:** Ongoing
- **Initiation date:** 2022-05-06
- **Report date:** 2022-06-01

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Miami, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0889-2022

## Citation

> AI Analytics. FDA recall D-0889-2022. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/D-0889-2022. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
