Lupin Pharmaceuticals Inc. recalls Lisinopril Tablets USP, 30 mg, 100-count bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore,
Lupin Pharmaceuticals recalls 30mg Lisinopril tablets due to foreign 5mg tablets found in some bottles. This may cause incorrect dosing. Check your bottle's lot number and contact the company for details.
Lower-risk recall
Presence of Foreign Tablet/ Capsule: Product complaint received indicating mix-up of one lisinopril 5mg tablet inside of a 30 mg, 100-count bottle of Lisinopril Tablets.
Contact the company & request your remedy
What happened, in plain English
Lupin Pharmaceuticals is recalling 30mg Lisinopril tablets because some bottles contain a 5mg tablet by mistake. This could lead to incorrect dosing if taken without noticing. Read more at govinfonow.com/recall/37203-lupin-lisinopril-30mg-tablets-recall-foreign-5mg-tablets-found.
Source Summary by GovInfoNow · govinfonow.com/recall/37203-lupin-lisinopril-30mg-tablets-recall-foreign-5mg-tablets-found · Updated October 5, 2026 · FDA enforcement record: FDA #D-1079-2020
Cite this page
“Lupin Lisinopril 30mg Tablets Recall: Foreign 5mg Tablets Found.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/37203-lupin-lisinopril-30mg-tablets-recall-foreign-5mg-tablets-found. Based on FDA recall #D-1079-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1079-2020%22&limit=1).
Why it’s dangerous
The product contains a 5mg lisinopril tablet inside a 30mg bottle by mistake. This could cause incorrect dosing if the 5mg tablet is taken instead of the intended 30mg dose.
Who’s affected
People who have the 30mg Lisinopril tablets with lot number Q900580 (expiring 9/2021) are affected. Those taking the medication for blood pressure are most at risk.
How to tell if you have this one
Check for the lot number Q900580 on the bottle. The product is a 30mg Lisinopril tablet, 100-count bottle, Rx only, manufactured in Baltimore, Maryland.
- Brand
Lupin Pharmaceuticals- Category
Drug
What to do — step by step
Check Your Bottle
Look for the lot number Q900580 on the bottle label. If it matches, the product is part of the recall.
Questions people ask
Is this product dangerous?
The recall is due to a mix-up of a 5mg tablet inside a 30mg bottle, which could lead to incorrect dosing. However, the risk is low as the issue is a manufacturing error, not a safety hazard.
How do I know if I have the recalled product?
Check the lot number on the bottle. The recalled product has lot number Q900580 and expires 9/2021.
What should I do if I have the recalled product?
The recall does not specify a remedy, so contact Lupin Pharmaceuticals for guidance.
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-1079-2020 — Lupin Pharmaceuticals Lupin Pharmaceuticals Hello, I own a Lupin Pharmaceuticals that is covered by recall D-1079-2020 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-1079-2020 (April 1, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1079-2020 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.