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Actavis Pharmaceuticals

No ongoing recalls currently shown

Based on the official records currently available to Public Health Trace, no recalls naming Actavis Pharmaceuticals are currently shown as ongoing. The 1 record below is a historical recall record.

Public Health Trace has 1 recall naming Actavis Pharmaceuticals as the recalling firm, republished from official FDA and USDA sources.

Recall history - 1 terminated record

Recalls by year

A bar chart of the number of recalls naming this company by year.

Recalls by year
YearRecalls
20131
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FDA Recall TerminatedTerminated: January 13, 2014Historical recordClass III

buPROPion Hydrochloride Extended - Release Tablets (XL) 300 mg, 30 tablet bottles, Rx Only, NDC 67767-142-30 Actavis Distributed by: Actavis South Atlantic LLC Sunrise, FL 33325 Packaged by by: America Health Packaging Columbus, OH 43217

by Actavis Pharmaceuticals

Reason
Failed Dissolution Specifications; 8-hours for the 18-month stability testing point.
Published
March 6, 2013
Distribution
Nationwide

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Showing 1–1 of 1 results

Some FDA recall records on this page come from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

This page lists recalls that name Actavis Pharmaceuticals as the recalling firm in the official source notice. It is not a safety rating, ranking, or statement that the company acted negligently. Read the full medical disclaimer.