NATCO Pharma Limited recalls Lansoprazole Delayed-Release Capsules USP, 15 mg, Acid reducer 24 Hour, Treats Frequent Heartburn, 14 capsules per
Natco Pharma recalls 15mg Lansoprazole capsules due to manufacturing deviations. Affected lots: 411988, expiring 05/31/2025. No immediate action needed but check your bottle.
Lower-risk recall
CGMP Deviations
Contact the company & request your remedy
What happened, in plain English
Natco Pharma is recalling 15mg Lansoprazole Delayed-Release Capsules because of manufacturing deviations. This could affect product safety, but the recall doesn't require immediate action. Read more at govinfonow.com/recall/32754-natco-pharma-lansoprazole-capsules-recall-cgmp-deviations-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/32754-natco-pharma-lansoprazole-capsules-recall-cgmp-deviations-risk · Updated September 23, 2026 · FDA enforcement record: FDA #D-0438-2024
Cite this page
“Natco Pharma Lansoprazole Capsules Recall: CGMP Deviations Risk.” GovInfoNow, updated September 23, 2026. https://govinfonow.com/recall/32754-natco-pharma-lansoprazole-capsules-recall-cgmp-deviations-risk. Based on FDA recall #D-0438-2024 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0438-2024%22&limit=1).
Why it’s dangerous
The recall is for CGMP (current good manufacturing practice) deviations, which means the product may not be made safely. This could lead to inconsistent drug quality, but the risk is not severe enough to cause serious injury.
Who’s affected
People who bought the recalled capsules from Rising Pharma Holdings in the US. Those with heartburn treatment needs are most at risk if they use the product.
How to tell if you have this one
Check for the NDC code 16571-742-41 and lot number 411988 on the bottle. The capsules are labeled as 15mg Lansoprazole Delayed-Release for heartburn relief.
- Brand
Natco Pharma- Category
Drug
What to do — step by step
Check Your Bottle
Look for the NDC code 16571-742-41 and lot number 411988 on the bottle label.
Questions people ask
Is this product dangerous?
The recall is for manufacturing deviations, but the product is not considered dangerous. No immediate action is needed.
How do I know if I have the recalled product?
Check for the NDC code 16571-742-41 and lot number 411988 on the bottle label.
Do I need to stop using the product?
No, the recall does not require stopping use. You can continue using the product if you have a different lot number.
Contact Natco Pharma
We’ve drafted a message you can send Natco Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0438-2024 — Natco Pharma Natco Pharma Hello, I own a Natco Pharma that is covered by recall D-0438-2024 from Natco Pharma. 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-0438-2024 (March 27, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0438-2024 to see it in context.
- Plain-language summary written by qwen3:4b on September 23, 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.