Dr. Reddy's recalls 1mg Varenicline tablets due to subpotent drug levels found in a specific lot during stability testing. This may affect prescription medication efficacy.
Sub potent drug: during the 9-month stability test conducted, the assay value for the affected lot was below specification limit.
Dr. Reddy's is recalling 1mg Varenicline tablets that may have lower-than-stated drug potency. This could mean the medication isn't as effective as it should be for treating smoking cessation.
The stability test showed the drug concentration was below the required level. This means the medication might not work as intended for smoking cessation, but it does not pose an immediate safety risk like injury or death.
Prescription patients using the recalled lot number F2400244 of Varenicline tablets. Those with specific medical conditions requiring precise dosing may be at slightly higher risk.
Check your prescription label for the lot number F2400244 and expiration date 10/31/2026. The product is a 1mg Varenicline tablet, 56 tablets, sold by Dr. Reddy's Laboratories Inc. in Princeton, NJ.
Look for the lot number F2400244 and expiration date 10/31/2026 on the prescription label.
The recall is for potential reduced effectiveness, not safety risks. The product is still safe but may not work as intended for smoking cessation.
Check your prescription label for the lot number F2400244 and expiration date 10/31/2026. If you have this specific lot, contact your doctor for alternative treatment options.
Look for the lot number F2400244 and expiration date 10/31/2026 on the prescription label. The product is a 1mg Varenicline tablet, 56 tablets, sold by Dr. Reddy's Laboratories Inc. in Princeton, NJ.
We’ve drafted a message you can send Dr. Reddy's to request your refund or repair — edit it as you like.
Subject: Recall D-0219-2026 — Dr. Reddy's Dr. Reddy's Hello, I own a Dr. Reddy's that is covered by recall D-0219-2026 from Dr. Reddy's. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
