Ascend Laboratories recalls 90-count, 500-count, and 1000-count Atorvastatin Calcium 10mg tablets (Rx only) due to failed dissolution specifications. No remedy stated in recall notice.
Failed Dissolution Specifications
Ascend Laboratories is recalling 10mg Atorvastatin Calcium tablets in 90-count, 500-count, and 1000-count bottles because they failed dissolution specifications. This means the medication may not work as intended, potentially affecting treatment effectiveness.
The tablets failed dissolution specifications, meaning they may not dissolve properly in the body. This could lead to the medication not working as intended, potentially causing treatment failure for conditions like high cholesterol.
People who have the recalled 10mg Atorvastatin Calcium tablets (Rx only) in 90-count, 500-count, or 1000-count bottles. Those with high cholesterol or on statin therapy are most at risk of treatment failure.
Check for 90-count, 500-count, or 1000-count bottles of Atorvastatin Calcium 10mg tablets (Rx only) with NDC numbers 67877-511-90, 67877-511-05, or 67877-511-10. The recall includes specific lot numbers with expiration dates from July 2026 to February 2027.
Identify if your Atorvastatin Calcium 10mg tablets are in 90-count, 500-count, or 1000-count bottles with the listed NDC numbers.
The product failed dissolution specifications, meaning it may not dissolve properly in the body and could lead to treatment failure.
The recall notice does not specify a remedy, so contact your healthcare provider for advice on whether to continue using the medication.
Yes, the recall includes specific lot numbers with expiration dates from July 2026 to February 2027.
We’ve drafted a message you can send Ascend Laboratories to request your refund or repair — edit it as you like.
Subject: Recall D-0017-2026 — Ascend Laboratories Ascend Laboratories Hello, I own a Ascend Laboratories that is covered by recall D-0017-2026 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.
