# FDA recall D-1044-2020

> **Noven Therapeutics, LLC** · Class II · drug recall initiated 2020-03-02.

## Product

Daytrana (methylphenidate transdermal system) patches, Delivers 20 mg over 9 hours (2.2 mg/hr), 30-count box, Rx only, Manufactured for Noven Therapeutics, LLC. Miami, FL 33186, NDC 68968-5554-3

## Reason for recall

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

## Distribution

U.S.A. Nationwide

## Key facts

- **Recall number:** D-1044-2020
- **Recalling firm:** Noven Therapeutics, LLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2020-03-02
- **Report date:** 2020-03-25
- **Termination date:** 2023-05-18

- **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-1044-2020

## Citation

> AI Analytics. FDA recall D-1044-2020. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/D-1044-2020. Source: US FDA. Licensed CC0.

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