US Drug Recall Register
Class III · Low risk Terminated Initiated Aug 14, 2012 (14 years ago)

Prometh VC with Codeine Cough Syrup, CV, Each 5mL contains: Codeine phosphate 10mg…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

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

What was recalled

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

Recalling firm
Actavis Mid Atlantic LLC
NDC code
0472-1629-16
Origin
NC, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-006-2013

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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