Dr. Reddy's Montelukast Tablets Recall: Foreign Metoprolol Found
Dr. Reddy's recalls 1000-count Montelukast Sodium Tablets due to foreign metoprolol tablets found in some bottles. Consumers should check product details and contact the company for guidance.
Lower-risk recall
Presence of Foreign Tablet(s)/Capsule(s): A foreign tablet was found in a bottle of Montelukast Sodium Tablets, USP 10mg, identified as metoprolol 25 mg.
Contact the company
What happened, in plain English
Dr. Reddy's is recalling Montelukast Sodium Tablets (10 mg, 1000 count) because foreign metoprolol tablets were found in some bottles. This could cause unintended medication effects if taken. Read more at govinfonow.com/recall/33062-dr-reddy-s-montelukast-tablets-recall-foreign-metoprolol-found.
Source Summary by GovInfoNow · govinfonow.com/recall/33062-dr-reddy-s-montelukast-tablets-recall-foreign-metoprolol-found · Updated August 17, 2026 · FDA enforcement record: FDA #D-0086-2024
Cite this page
“Dr. Reddy's Montelukast Tablets Recall: Foreign Metoprolol Found.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/33062-dr-reddy-s-montelukast-tablets-recall-foreign-metoprolol-found. Based on FDA recall #D-0086-2024 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0086-2024%22&limit=1).
Why it’s dangerous
Foreign metoprolol tablets (a different medication) were found in some bottles of Montelukast Sodium Tablets. If someone takes the foreign tablets, they could experience unintended medication effects.
Who’s affected
People who have the 1000-count Montelukast Sodium Tablets (10 mg) from Dr. Reddy's, distributed by Dr. Reddy's Laboratories, Inc. in the U.S. are affected. Those with a prescription for this medication are most at risk.
How to tell if you have this one
Check for the product name 'Montelukast Sodium Tablets, USP 10 mg, Rx Only, 1000 count bottle' with NDC# 55111-725-10. The lot number is C2305569 and expiration date is 03/31/2026.
- Brand
Dr. Reddy's- Category
Drug
What to do — step by step
Check Product Details
Look for the NDC# 55111-725-10 and lot number C2305569 on the bottle.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 11 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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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-0086-2024 (October 13, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0086-2024 to see it in context.
- Plain-language summary written by qwen3:4b on August 17, 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.