Skip to main content

Actavis

No ongoing recalls currently shown

Based on the official records currently available to Public Health Trace, no recalls naming Actavis are currently shown as ongoing. The 3 records below are historical recall records.

Public Health Trace has 3 recalls naming Actavis as the recalling firm, republished from official FDA and USDA sources.

Recall history - 3 terminated records

Recalls by year

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

Recalls by year
YearRecalls
20121
20131
20141
Download CSV

FDA Recall TerminatedTerminated: September 5, 2014Historical recordClass III

Gelnique (oxybutynin chloride) Gel 10%, 100 mg in 1 g sachet, for topical use only. Physician sample in clamshell container with seven heat-sealed sachets. Rx Only. Watson Pharmaceuticals Inc, Corona, CA, 92890. NDC: 52544-084-77.

by Actavis

Reason
Subpotent Drug: Drug potency was compromised during shipment.
Published
March 5, 2014
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: April 9, 2014Historical recordClass III

Fentanyl Transdermal System, 50 mcg/h, 1 system per pouch (NDC 0591-3212-54), packaged in 5-count systems per box (NDC 0591-3212-72), Rx only, Manufactured by Watson Laboratories, Inc, Corona, CA, 92880 USA; Distributed by: Watson Pharma, Inc.

by Actavis

Reason
Failed Impurities/Degradation Specifications
Published
June 19, 2013
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: April 10, 2013Historical recordClass II

Fentanyl Transdermal System, 100 mcg/h, each transdermal system contains: 10 mg fentanyl and 0.4 mL alcohol USP, Rx only, supplied in single pouches (NDC 0591-3214-54 (pouch)), 5 pouches per carton (NDC 0591-3214-72 (Carton)), Manufactured by Watson laboratories Inc., Corona, CA, Distributed by: Watson, Pharma Inc.

by Actavis

Reason
Subpotent; some patches may not contain fentanyl gel
Published
October 3, 2012
Distribution
Nationwide

View recall →

Showing 1–3 of 3 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 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.