Ritussin DM Double Strength recalled over manufacturing violations

Recall date

May 31, 2019

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Official notice title

Geritrex, LLC recalls Ritussin DM Double Strength, 4 FL. OZ. (118 mL), RIJ Pharmaceutical Corporation 40 Commercial Avenue Middletown, NY 109…

Recall number

D-1525-2019

FDA classification

Class II

Brand / firm

Geritrex, LLC

Sold / distributed

U.S.A. Nationwide

Why it was recalled

cGMP Deviations: Products may have microbial contamination.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Ritussin DM Double Strength, 4 FL. OZ. (118 mL), RIJ Pharmaceutical Corporation 40 Commercial Avenue Middletown, NY 10941