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FDAFDA · Food and drugs·Recall number D-0500-2021

Livalo (pitavastatin) tablets 2 mg* Rx Only NdC 66869-204-90 Manufactured under license from: Kowa Company, Limited Tokyo 103-8433 Japan Tablets Manufactured by: Patheon, Inc. Cincinnati, OH 45237 USA or by Kowa Company, Ltd Nagoya 462-0024 Japan

Published June 2, 2021 · Recall initiated: March 15, 2021

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

CGMP Deviations: Intermittent exposure to temperature excursion during storage.

What to do

Voluntary: Firm initiated · Letter

Recall details

Brand
LIVALO
Manufacturer
Cardinal Health Inc.
Distributor
FL, GA, SC
UPC
0366869204905
Lot
3193479
Risk classification
Class II
Area (FDA)
drug
Country
United States

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