Amerisource Health Services recalls glipiZIDE Extended-Release Tablets 2.5mg 30-count due to failed dissolution specifications. This could affect medication effectiveness. Check your carton for lot number 1012910.
Failed Dissolution Specifications:
Amerisource Health Services is recalling glipiZIDE Extended-Release Tablets 2.5mg 30-count (3x10 blister cards) because they failed dissolution specifications. This means the medication might not work properly as intended.
The tablets failed dissolution specifications, which means they may not release medication properly in the body. This could lead to inconsistent blood pressure control. However, the recall does not indicate immediate harm to users.
Prescription holders of glipiZIDE Extended-Release Tablets 2.5mg 30-count with lot number 1012910 are affected. People taking this medication for blood pressure should be most concerned.
Check your glipiZIDE Extended-Release Tablets 2.5mg 30-count carton for lot number 1012910. The expiration date is April 30, 2025. This product was distributed by American Health Packaging in Columbus, Ohio.
Look for lot number 1012910 on the carton of glipiZIDE Extended-Release Tablets 2.5mg 30-count.
The recall indicates failed dissolution specifications, which could affect medication effectiveness. However, the product is not considered immediately dangerous.
Check the lot number on your carton. If it matches 1012910, contact Amerisource Health Services for further instructions.
Look for lot number 1012910 on the carton of glipiZIDE Extended-Release Tablets 2.5mg 30-count with expiration date 04/30/2025.
We’ve drafted a message you can send Amerisource Health Services to request your refund or repair — edit it as you like.
Subject: Recall D-0202-2025 — Amerisource Health Services Amerisource Health Services Hello, I own a Amerisource Health Services that is covered by recall D-0202-2025 from Amerisource Health Services. 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.
