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Actavis Mid Atlantic LLC

No ongoing recalls currently shown

Based on the official records currently available to Public Health Trace, no recalls naming Actavis Mid Atlantic LLC are currently shown as ongoing. The 2 records below are historical recall records.

Public Health Trace has 2 recalls naming Actavis Mid Atlantic LLC as the recalling firm, republished from official FDA and USDA sources.

Recall history - 2 terminated records

Recalls by year

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

Recalls by year
YearRecalls
20122
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FDA Recall TerminatedTerminated: June 27, 2013Historical recordClass III

Prometh VC with Codeine Cough Syrup, CV, Each 5mL contains: Codeine phosphate 10mg; promethazine hydrochloride 6.25mg; phenylephrine hydrochloride 5mg, One Pint Bottles (473mL), Rx Only, Manufactured by: Actavis Mid Atlantic LLC., 1877 Kawaii Road, Lincolnton, NC 28092 USA, NDC 0472-1629-16

by Actavis Mid Atlantic LLC

Reason
Impurities/Degradation Products: Recalled lots do not meet room temperature stability specification for unknown degradant.
Published
October 17, 2012
Distribution
Nationwide

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FDA Recall TerminatedTerminated: June 27, 2013Historical recordClass III

Prometh VC Plain, Each 5mL contains: Promethazine Hydrochloride 6.25mg & Phenylephrine Hydrochloride 5mg, One Pint Bottles (473mL), Rx Only, Manufactured by: Actavis Mid Atlantic, LLC., 1877 Kawaii Road, Lincolnton, NC, 28092, USA, NDC 0472-1628-16.

by Actavis Mid Atlantic LLC

Reason
Impurities/Degradation Products: Recalled lots do not meet room temperature stability specification for unknown degradant.
Published
October 17, 2012
Distribution
Nationwide

View recall →

Showing 1–2 of 2 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 Mid Atlantic LLC 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.