Rising Pharma recalls Duloxetine DR Capsules 60mg bottles due to N-nitroso-duloxetine impurity exceeding safety limits. Consumers should check lot numbers and contact the company for details.
CGMP Deviations; Presence of N-nitroso-duloxetine impurity above recommended interim limit.
Rising Pharma is recalling Duloxetine DR Capsules 60mg bottles that contain an impurity above safe levels. This could pose a health risk if taken, so affected consumers should stop using the product and contact the company.
The capsules contain N-nitroso-duloxetine impurities at levels higher than the recommended safety limit. This impurity could cause health issues if the medication is taken as directed.
People who have the 60mg Duloxetine capsules with specific lot numbers and expiration dates listed in the recall notice are affected. Those taking this medication for depression or nerve pain are at highest risk.
Check the product label for the lot numbers: DT6023053A through DT6023048A with expiration dates from December 2024 to January 2025. The product is sold in 30-count and 1000-count bottles.
Immediately stop taking the recalled Duloxetine capsules if you have them.
Reach out to Rising Pharma for further instructions on returning the product.
Lot numbers DT6023053A, DT6023061A, DT6023068A, DT6023074A, DT6023078A, DT6023076A, DTC24043A, DTC24044A, DT6023002A, DT6023016A, DT6023036A, DT6023048A.
The product was distributed with specific expiration dates from December 2024 to January 2025.
Check the product label for the lot numbers listed in the recall notice.
We’ve drafted a message you can send Rising Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0190-2025 — Rising Pharma Rising Pharma Hello, I own a Rising Pharma that is covered by recall D-0190-2025 from Rising Pharma. 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.
