Ascend Laboratories recalls 20mg Atorvastatin Calcium Tablets with failed dissolution specifications. These tablets may not release medication properly, risking ineffective treatment. Check NDC codes and expiration dates for affected lots.
Failed Dissolution Specifications
Ascend Laboratories is recalling 20mg Atorvastatin Calcium Tablets due to failed dissolution specifications. This means the tablets may not release medication properly, potentially leading to ineffective treatment. The recall covers specific lot numbers and expiration dates.
The tablets failed dissolution specifications, meaning they may not release medication properly when taken. This could result in ineffective treatment for cholesterol management. The risk is related to the medication not working as intended, not immediate harm.
People who have the recalled 20mg Atorvastatin Calcium Tablets with specific NDC codes and expiration dates. Those on cholesterol-lowering medication are most at risk if the tablets don't work as intended.
Check for NDC codes 67877-512-90, 67877-512-05, or 67877-512-10 on the packaging. The affected lots have expiration dates from June 2026 to December 2026.
Look for the NDC codes 67877-512-90, 67877-512-05, or 67877-512-10 on the packaging.
The tablets failed dissolution specifications, meaning they may not release medication properly, potentially leading to ineffective treatment.
Check the NDC codes and expiration dates on the packaging to see if your product is affected. If it is, contact your healthcare provider for guidance.
The recall is due to potential ineffective treatment, not immediate safety risks. The risk is related to the medication not working as intended.
We’ve drafted a message you can send Ascend Laboratories to request your refund or repair — edit it as you like.
Subject: Recall D-0019-2026 — Ascend Laboratories Ascend Laboratories Hello, I own a Ascend Laboratories that is covered by recall D-0019-2026 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.
