Actavis Mid Atlantic LLC Recalls

Overview of recall records associated with Actavis Mid Atlantic LLC, including dates, categories and classifications where available.

2recall records

Oct 17, 2012latest record date

Oct 17, 2012earliest record date

Recall history in this database

Classification mix: Class III: 2.

DrugOct 17, 2012

Actavis Mid Atlantic Prometh VC Plain, Each 5mL contains: Promethazine Hydrochloride 6.25mg recall — FDA D-005-2013

Impurities/Degradation Products: Recalled lots do not meet room temperature stability specification for unknown degradant.

Class IIIFDA: TerminatedActavis Mid Atlantic LLC

DrugOct 17, 2012

Actavis Mid Atlantic Prometh VC with Codeine Cough Syrup, CV, Each 5mL contains: Codeine recall — FDA D-006-2013

Impurities/Degradation Products: Recalled lots do not meet room temperature stability specification for unknown degradant.

Class IIIFDA: TerminatedActavis Mid Atlantic LLC

Understanding this recall history

This page summarizes recall records in which the official source identifies Actavis Mid Atlantic LLC as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.