Actavis Mid Atlantic recalls
Actavis Mid Atlantic appears in 2 official U.S. recall notices indexed by RecallRadar, most recently on 2012-10-17.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
Recall summary
| Recall notices | 2 |
|---|---|
| Published | 2012-10-17 |
| By agency | FDA Drug (2) |
| By classification | Class III (2) |
| By status | terminated (2) |
| Distribution named in notices | US |
Recalls
- Prometh VC Plain, Each 5mL contains: Promethazine Hydrochloride 6.25mg & Phenylephrine Hydrochloride 5mg, One Pint Bottles (473mL), Rx Only…
FDA Drug · Class III · 2012-10-17 · Actavis Mid Atlantic
Reason: Impurities/Degradation Products: Recalled lots do not meet room temperature stability specification for unknown degradant. - Prometh VC with Codeine Cough Syrup, CV, Each 5mL contains: Codeine phosphate 10mg
FDA Drug · Class III · 2012-10-17 · Actavis Mid Atlantic
Reason: Impurities/Degradation Products: Recalled lots do not meet room temperature stability specification for unknown degradant.