US Drug Recall Register
Class II · Moderate risk Terminated Initiated May 31, 2019 (7 years ago)

Ritussin DM Double Strength, 4 FL. OZ. (118 mL), RIJ Pharmaceutical Corporation 40…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

cGMP Deviations: Products may have microbial contamination.

What was recalled

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

Recalling firm
Geritrex, LLC
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1525-2019

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.