FDA recall D-1525-2019
Geritrex, LLC · Class II · drug
Product
Ritussin DM Double Strength, 4 FL. OZ. (118 mL), RIJ Pharmaceutical Corporation 40 Commercial Avenue Middletown, NY 10941
Reason for recall
cGMP Deviations: Products may have microbial contamination.
Distribution
U.S.A. Nationwide
Key facts
- Status
- Terminated
- Initiation date
- 2019-05-31
- Report date
- 2019-07-31
- Termination date
- 2024-02-02
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Middletown, NY, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1525-2019