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

FDA recall notice · announced July 31, 2019 · Ucb

Class II FDA/FSIS Class II: use may cause temporary or medically reversible adverse health consequences.

The 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.

Notes

Distribution: TN
Lot/code information: Lot: 908946 Exp. 02/2022
Quantity: 2088 bottles
Status: Terminated
Products in this recall event:
- Keppra (levetiracetam) 1000 mg tablets, 60 tablets per bottle, Rx only, Manufactured for UCB, Inc. Smyrna, GA 30080, NDC 50474-597-66. (D-1838-2019)

Source: U.S. Food and Drug Administration public recall data. This page reports official records and is not legal, medical, or repair advice.