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Actavis Mid Atlantic LLC

Recalls

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 Terminated Historical 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 Terminated Historical 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

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Showing 1–2 of 2 results

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.