RIJ Pharmaceutical LLC recalls Ritussin DM Dextromethorphan Hydrobormide (Dextromethorphan HBr, USP 10 mg, Guaifenesin, USP 100mg), packaged in 4 FL.OZ
Recalled June 20, 2018 · FDA recall D-0849-2018 · RIJ Pharmaceutical
Hazard
CGMP Deviations: Products are being recalled due to an out of specification total aerobic microbial count in a water sample. · FDA Class II
Units
9240 bottles
Sold at
Nationwide in the USA
Description
CGMP Deviations: Products are being recalled due to an out of specification total aerobic microbial count in a water sample.
Product
Ritussin DM Dextromethorphan Hydrobormide (Dextromethorphan HBr, USP 10 mg, Guaifenesin, USP 100mg), packaged in 4 FL.OZ. (118 mL), RIJ PHARMACEUTICAL CORPORATION 40 COMMERCIAL AVENUE, MIDDLETOWN, NY 10941, NDC 5380740904, UPC 35380740941
Manufacturer(s)
RIJ Pharmaceutical LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →