FDA recall record

ALLERGAN Viokace (pancrelipase) tablets, 20,880 USP units, 100-count bottle recall — FDA D-0154-2018

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

Class IIclassification
D-0154-2018official record ID
Jan 17, 2018report date

Recall record at a glance

Official recordD-0154-2018
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmALLERGAN
Report dateJan 17, 2018
Recall initiation dateDec 4, 2017
Quantity12,699 bottles
LocationMadison, NJ, United States

Official product description

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

Why the product was recalled

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

Distribution information

U.S.A. nationwide

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.

DrugFeb 21, 2018

ALLERGAN NORCO recall — FDA D-0413-2018

Labeling: Not Elsewhere Classified: does not have the required "CII" controlled drug classification indication on the primary label.

Class IIIFDA: TerminatedALLERGAN