RecallDepth
Class II Terminated

Viokace (pancrelipase) tablets, 20,880 USP units, 100-count bottle, Rx only, Distributed by; Allergan USA Inc., Irvine, CA 92612, Manufactured in Canada, NDC 58914-117-10

This recall has been terminated (originally issued January 17, 2018).

Company
Allergan
Recall Initiated
December 4, 2017
Posted
January 17, 2018
Recall Number
D-0154-2018
Voluntary / Mandated
Voluntary: Firm initiated
Quantity
12,699 bottles
Firm Location
Madison, NJ, United States
Official Source
View on FDA website ↗

Reason for Recall

Subpotent Drug: One lot of Viokace is being recalled since product stability testing results did not meet the specifications for enzyme profile.

Distribution

U.S.A. nationwide

Lot / Code Info

Lot #: 160741A, Exp 02/18

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