The Harvard Drug Group recalls Aripiprazole Tablets, USP, 15 mg, 30 tablets per unit dose carton, Rx Only, Manufactured by: Apotex, Inc, Toronto,
Harvard Drug Group recalls 15mg Aripiprazole tablets with failed dissolution specs. Affected lots T02520 and T02637 expired 02/2021. No remedy stated in recall notice.
Recall notice
Failed Dissolution Specifications: Out of specification for dissolution.
Contact the company & request your remedy
What happened, in plain English
The Harvard Drug Group is recalling Aripiprazole 15mg tablets that failed dissolution testing. This means the medication may not work as intended when taken. People with prescriptions for this drug should check if their tablets are in the affected lots. Read more at govinfonow.com/recall/36668-harvard-drug-group-recalls-aripiprazole-15mg-tablets-due-to-dissolution.
Source Summary by GovInfoNow · govinfonow.com/recall/36668-harvard-drug-group-recalls-aripiprazole-15mg-tablets-due-to-dissolution · Updated October 4, 2026 · FDA enforcement record: FDA #D-0114-2021
Cite this page
“Harvard Drug Group recalls Aripiprazole 15mg tablets due to dissolution failure.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/36668-harvard-drug-group-recalls-aripiprazole-15mg-tablets-due-to-dissolution. Based on FDA recall #D-0114-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0114-2021%22&limit=1).
Why it’s dangerous
The tablets failed dissolution specifications, meaning they may not release the medication properly in the body. This could lead to the drug not working as intended. However, the recall does not specify if this causes serious harm.
Who’s affected
People with prescriptions for Aripiprazole 15mg tablets from this recall. Those who have the specific lots T02520 or T02637 (expired 02/2021) are most at risk.
How to tell if you have this one
Check your prescription label for the lot numbers T02520 or T02637. The tablets were manufactured by Apotex, Inc in Toronto, Canada and distributed by Major Pharmaceuticals in Livonia, Michigan.
- Brand
The Harvard Drug Group- Category
Drug
What to do — step by step
Check Your Tablets
Look for lot numbers T02520 or T02637 on the packaging. The tablets were manufactured by Apotex, Inc in Toronto, Canada.
Questions people ask
Do I need to stop using these tablets?
The recall does not specify a remedy, so you do not need to stop using them immediately.
What should I do if I have these tablets?
The official recall notice does not state any action steps for affected tablets.
Are there any safety risks from these tablets?
The recall mentions failed dissolution specifications, but does not describe any specific safety risks.
Contact The Harvard Drug Group
We’ve drafted a message you can send The Harvard Drug Group to request your refund or repair — edit it as you like.
Subject: Recall D-0114-2021 — The Harvard Drug Group The Harvard Drug Group Hello, I own a The Harvard Drug Group that is covered by recall D-0114-2021 from The Harvard Drug Group. 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-0114-2021 (November 18, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0114-2021 to see it in context.
- Plain-language summary written by qwen3:4b on October 4, 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.