# FDA recall D-1838-2019

> **Ucb, Inc** · Class II · drug recall initiated 2019-07-18.

## Product

Keppra (levetiracetam) 1000 mg tablets, 60 tablets per bottle,  Rx only, Manufactured for UCB, Inc. Smyrna, GA 30080, NDC 50474-597-66.

## Reason for recall

Failed Dissolution Specifications.

## Distribution

TN

## Key facts

- **Recall number:** D-1838-2019
- **Recalling firm:** Ucb, Inc
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2019-07-18
- **Report date:** 2019-07-31
- **Termination date:** 2020-01-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Smyrna, GA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1838-2019

## Citation

> AI Analytics. FDA recall D-1838-2019. Retrieved 2026-06-16 from https://api.ai-analytics.org/recall/D-1838-2019. Source: US FDA. Licensed CC0.

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