American Health Packaging recalls GlipiZIDE Extended-release Tablets, 2.5 mg, 30 Tablets (3 x 10), Rx Only, Packaged and Distributed by: American Health
American Health Packaging recalls GlipiZIDE Extended-release Tablets due to dissolution failure at time zero, potentially affecting drug release. Check NDC 68084-295-21 and lot 181288.
Lower-risk recall
Failed Dissolution Specifications: dissolution failure at time zero of the repackaged lot. Drug release results were slightly above specification at time zero.
Contact the company & request your remedy
What happened, in plain English
American Health Packaging recalls GlipiZIDE Extended-release Tablets (2.5 mg, 30 tablets) because they failed dissolution tests at time zero. This could mean the medication doesn't release properly when taken, which might affect treatment effectiveness. Read more at govinfonow.com/recall/38946-american-health-glipizide-extended-release-tablets-recall-dissolution-failure-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/38946-american-health-glipizide-extended-release-tablets-recall-dissolution-failure-risk · Updated October 5, 2026 · FDA enforcement record: FDA #D-1276-2019
Cite this page
“American Health GlipiZIDE Extended-release Tablets Recall: Dissolution Failure Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/38946-american-health-glipizide-extended-release-tablets-recall-dissolution-failure-risk. Based on FDA recall #D-1276-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1276-2019%22&limit=1).
Why it’s dangerous
The tablets failed dissolution tests at time zero, meaning they didn't release the medication properly when first exposed to water. This could lead to inconsistent drug levels in the body, potentially reducing effectiveness.
Who’s affected
People with a prescription for GlipiZIDE Extended-release Tablets who received this specific lot (NDC 68084-295-21, lot 181288) are affected. Those taking blood pressure medication are most at risk if the tablets don't dissolve correctly.
How to tell if you have this one
Check for the NDC code 68084-295-21 and lot number 181288 on the packaging. The product was distributed by American Health Packaging and sold with an expiration date of May 31, 2020.
- Brand
American Health Packaging- Category
Drug
What to do — step by step
Check Product Details
Look for NDC 68084-295-21 and lot number 181288 on the packaging.
Questions people ask
Is this product safe to take?
The recall is due to dissolution failure at time zero, which may affect medication release. Consult your doctor or pharmacist for advice on whether to continue using the product.
How can I check if I have the recalled product?
Check the NDC code 68084-295-21 and lot number 181288 on the packaging. The product was distributed by American Health Packaging with an expiration date of May 31, 2020.
What should I do if I have the recalled product?
The recall record does not specify a remedy, so contact your doctor or pharmacist for guidance on next steps.
Contact American Health 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-1276-2019 — American Health Packaging American Health Packaging Hello, I own a American Health Packaging that is covered by recall D-1276-2019 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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Where this comes from
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.
- Official source: FDA Recall #D-1276-2019 (April 8, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1276-2019 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.