American Health Packaging recalls GlipiZIDE Extended-Release Tablets (2.5 mg, 30 tablets) due to failed dissolution specifications. This may affect medication effectiveness. Check carton NDC 68084-295-21 and lot number 194141.
Failed Dissolution Specifications: results were above specification.
American Health Packaging is recalling GlipiZIDE Extended-Release Tablets (2.5 mg, 30 tablets) because they failed dissolution specifications. This could mean the medication doesn't work as intended, so users should check if they have the recalled product.
The tablets failed dissolution specifications, meaning they may not release the medication correctly in the body. This could lead to inconsistent blood pressure control. However, the recall is for prescription use only and does not indicate immediate harm.
Prescription drug users who have the recalled GlipiZIDE Extended-Release Tablets (2.5 mg, 30 tablets) with carton NDC 68084-295-21 and lot number 194141. People taking blood pressure medication are most at risk if the tablets don't dissolve properly.
Check for the carton NDC number 68084-295-21 and lot number 194141 on the product packaging. The product is prescription-only and sold in blister packs with 30 tablets per carton.
Look for the carton NDC number 68084-295-21 and lot number 194141 on the product packaging.
The recall is due to failed dissolution specifications, which may affect medication effectiveness. If you have the recalled product, you should check with your doctor or pharmacist.
The recall does not specify a remedy, so you should check with your doctor or pharmacist for guidance.
Check for the carton NDC number 68084-295-21 and lot number 194141 on the product packaging.
We’ve drafted a message you can send American Health Packaging to request your refund or repair — edit it as you like.
Subject: Recall D-0020-2022 — American Health Packaging American Health Packaging Hello, I own a American Health Packaging that is covered by recall D-0020-2022 from American Health Packaging. 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.
