Lupin Pharmaceuticals Inc. recalls Lisinopril Tablets, USP, 5 mg, Rx Only, 1000-count bottle, Manufactured for: Lupin Pharmaceuticals Inc., Baltimore, MD
Lupin Pharmaceuticals recalls 5mg Lisinopril tablets due to mix-up with 10mg tablets. Affected bottles may contain incorrect strength.
Lower-risk recall
Product Mix Up: Lisinopril 10 mg tablets were found in Lisinopril 5 mg 1000-count bottle.
Contact the company & request your remedy
What happened, in plain English
Lupin Pharmaceuticals is recalling 5mg Lisinopril tablets because some bottles contain 10mg tablets instead of 5mg. This mix-up could lead to incorrect dosing if taken without knowing the actual strength. Read more at govinfonow.com/recall/37094-lupin-lisinopril-5mg-tablets-recall-product-mix-up-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/37094-lupin-lisinopril-5mg-tablets-recall-product-mix-up-risk · Updated October 5, 2026 · FDA enforcement record: FDA #D-1290-2020
Cite this page
“Lupin Lisinopril 5mg Tablets Recall: Product Mix-Up Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/37094-lupin-lisinopril-5mg-tablets-recall-product-mix-up-risk. Based on FDA recall #D-1290-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1290-2020%22&limit=1).
Why it’s dangerous
The product mix-up means some 5mg bottles contain 10mg tablets. If taken without realizing the tablet strength, users could receive a higher dose than prescribed, potentially causing adverse effects.
Who’s affected
Prescription users of Lisinopril 5mg tablets who received this specific bottle. Those with a history of hypertension or heart conditions are at slightly higher risk due to potential dosing errors.
How to tell if you have this one
Check for the bottle label showing 'Lisinopril Tablets, USP, 5 mg, Rx Only, 1000-count'. Look for the lot number Q900683 and expiration date 10/31/2022.
- Brand
Lupin Pharmaceuticals- Category
Drug
What to do — step by step
Check Tablet Strength
Verify the tablet strength by checking the label for '5 mg' or '10 mg' on the bottle.
Questions people ask
Why is this product being recalled?
Lupin Pharmaceuticals found that some 5mg Lisinopril tablets were mixed up with 10mg tablets in the same bottle.
How can I tell if I have the recalled product?
Check for the label 'Lisinopril Tablets, USP, 5 mg, Rx Only, 1000-count' with lot number Q900683 and expiration date 10/31/2022.
What should I do if I have the recalled product?
The recall does not require immediate action; check the tablet strength before use.
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-1290-2020 — Lupin Pharmaceuticals Lupin Pharmaceuticals Hello, I own a Lupin Pharmaceuticals that is covered by recall D-1290-2020 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-1290-2020 (May 28, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1290-2020 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.