Ascend Laboratories recalls 40mg Atorvastatin Calcium Tablets (NDC 67877-513-90, 67877-513-05, 67877-513-10) due to failed dissolution specifications. Consumers should contact the manufacturer for details.
Failed Dissolution Specifications
Ascend Laboratories has recalled certain 40mg Atorvastatin Calcium Tablets because they failed dissolution specifications. This means the medication may not work as intended when taken. The recall affects specific lot numbers and quantities.
The tablets failed dissolution specifications, meaning they may not dissolve properly in the body. This could lead to the medication not working as intended when taken. However, the recall does not indicate a risk of serious injury or death.
People who have the recalled 40mg Atorvastatin Calcium Tablets (NDC 67877-513-90, 67877-513-05, 67877-513-10) from Alkem Laboratories in India, distributed by Ascend Laboratories in the U.S. are affected. Those taking this medication for cholesterol management are most at risk.
Check the product label for the NDC codes 67877-513-90, 67877-513-05, or 67877-513-10. The lot numbers listed are 25140933 (exp. Feb 2027), 25140477 (exp. Dec 2026), 24144254 (exp. Oct 2026), 24144163 (exp. Sep 2026), and 24143995 (exp. Sep 2026).
Look for the NDC codes 67877-513-90, 67877-513-05, or 67877-513-10 on the label.
The tablets failed dissolution specifications, meaning they may not dissolve properly in the body and could not work as intended when taken.
Lot numbers 25140933 (exp. Feb 2027), 25140477 (exp. Dec 2026), 24144254 (exp. Oct 2026), 24144163 (exp. Sep 2026), and 24143995 (exp. Sep 2026).
Check the product label for the NDC codes 67877-513-90, 67877-513-05, or 67877-513-10.
We’ve drafted a message you can send Ascend Laboratories to request your refund or repair — edit it as you like.
Subject: Recall D-0018-2026 — Ascend Laboratories Ascend Laboratories Hello, I own a Ascend Laboratories that is covered by recall D-0018-2026 from Ascend Laboratories. 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.
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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.
