Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
Sub potent drug: during the 9-month stability test conducted, the assay value for the affected lot was below specification limit.
What was recalled
Varenicline Tablets, 1mg, 56 Tablets, Rx only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, NDC 43598-908-56
Recalling firm
Dr. Reddy's Laboratories, Inc.
NDC code
43598-908-56
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0219-2026
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.