Lupin Pharmaceuticals Inc. recalls Lisinopril Tablets USP, 10 mg, 1000 count bottles, Manufactured by: Lupin Limited, Nagpur INDIA, For BluePoint
Lupin Pharmaceuticals recalls 10mg Lisinopril tablets due to foreign 20mg tablets in some bottles. Affected lots may contain unsafe medication.
Lower-risk recall
Presence of Foreign Tablets/Capsules: Lisinopril Tablets USP, 20mg found in a 1000 count bottle of Lisinopril Tablets USP, 10mg
Contact the company & request your remedy
What happened, in plain English
Lupin Pharmaceuticals is recalling 1000-count bottles of 10mg Lisinopril tablets after finding 20mg tablets in some batches. This could lead to incorrect dosing if taken. Read more at govinfonow.com/recall/36930-lupin-lisinopril-10mg-tablets-recall-foreign-20mg-tablets-found.
Source Summary by GovInfoNow · govinfonow.com/recall/36930-lupin-lisinopril-10mg-tablets-recall-foreign-20mg-tablets-found · Updated October 5, 2026 · FDA enforcement record: FDA #D-1413-2020
Cite this page
“Lupin Lisinopril 10mg Tablets Recall: Foreign 20mg Tablets Found.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/36930-lupin-lisinopril-10mg-tablets-recall-foreign-20mg-tablets-found. Based on FDA recall #D-1413-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1413-2020%22&limit=1).
Why it’s dangerous
The recall involves 20mg tablets mistakenly included in 10mg bottles. Taking these could cause incorrect dosing, potentially leading to health issues if not managed properly.
Who’s affected
People who own or use Lupin's 10mg Lisinopril tablets from the specified lot numbers. Those taking the medication for blood pressure are most at risk.
How to tell if you have this one
Check for the lot number Q000232 on the bottle. The product was sold by BluePoint Laboratories with NDC 68001-334-08 and expired January 2022.
- Brand
Lupin Pharmaceuticals- Category
Drug
What to do — step by step
Check Your Product
Look for the lot number Q000232 on the bottle label.
Questions people ask
Why is this product being recalled?
Lupin Pharmaceuticals found 20mg tablets in some 1000-count bottles of 10mg Lisinopril tablets.
What should I do if I have this product?
Check the lot number on the bottle. If it's Q000232, contact Lupin Pharmaceuticals for guidance.
Is this dangerous?
The recall is for potential incorrect dosing, but the risk is low if you check the lot number and take appropriate action.
Contact Lupin Pharmaceuticals
We’ve drafted a message you can send Lupin Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-1413-2020 — Lupin Pharmaceuticals Lupin Pharmaceuticals Hello, I own a Lupin Pharmaceuticals that is covered by recall D-1413-2020 from Lupin Pharmaceuticals. 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-1413-2020 (July 17, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1413-2020 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.