AMERICAN HEALTH PACKAGING recalls Aripiprazole Tablets, USP, 10 mg, 100 Tablets (10 x 10) unit dose blisters [NDC60687-179-11; UPC (01) 003 60687 179 11
American Health Packaging recalls 10 mg Aripiprazole tablets due to CGMP deviations affecting quality. No remedy specified in official notice.
Recall notice
CGMP Deviations: lot made with active pharmaceutical ingredient that did not meet all its intended specifications.
Contact the company & request your remedy
What happened, in plain English
American Health Packaging is recalling 10 mg Aripiprazole tablets that were made with active pharmaceutical ingredients not meeting all intended specifications. This could affect product safety and effectiveness. Read more at govinfonow.com/recall/40923-american-health-packaging-aripiprazole-tablets-recall-cgmp-deviations.
Source Summary by GovInfoNow · govinfonow.com/recall/40923-american-health-packaging-aripiprazole-tablets-recall-cgmp-deviations · Updated October 7, 2026 · FDA enforcement record: FDA #D-0595-2018
Cite this page
“American Health Packaging Aripiprazole Tablets Recall: CGMP Deviations.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/40923-american-health-packaging-aripiprazole-tablets-recall-cgmp-deviations. Based on FDA recall #D-0595-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0595-2018%22&limit=1).
Why it’s dangerous
The manufacturing process failed to meet quality standards for the active ingredient, which could lead to inconsistent medication effectiveness or safety issues. This is a CGMP deviation, meaning the product did not meet regulatory requirements for quality.
Who’s affected
People who have the recalled 10 mg Aripiprazole tablets (NDC 60687-179-11) from American Health Packaging. Those with mental health conditions requiring this medication are most at risk.
How to tell if you have this one
Check for the product name 'Aripiprazole Tablets, USP, 10 mg, 100 Tablets (10 x 10) unit dose blisters' with NDC 60687-179-11. The lot number 174096 was distributed by American Health Packaging in Columbus, Ohio.
- Brand
American Health Packaging- Category
Drug
What to do — step by step
Check Product Details
Identify the product by checking the NDC code 60687-179-11 and lot number 174096 on the packaging.
Questions people ask
Is there a remedy for this recall?
The official notice does not specify a remedy.
What is the specific problem with these tablets?
The manufacturing process had CGMP deviations, meaning the active pharmaceutical ingredient did not meet all intended specifications.
How can I tell if I have the recalled product?
Look for the NDC code 60687-179-11 and lot number 174096 on the packaging.
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-0595-2018 — American Health Packaging American Health Packaging Hello, I own a American Health Packaging that is covered by recall D-0595-2018 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-0595-2018 (January 19, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0595-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 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.