Dr. Reddy's Metoprolol Tablets Recall: Foreign Clopidogrel Tablets Found
Dr. Reddy's recalls 100-mg Metoprolol Succinate Extended-Release Tablets due to foreign Clopidogrel tablets found in some bottles. This is a prescription-only product.
Lower-risk recall
Presence of Foreign Tablets/Capsules: One foreign tablet identified as Clopidogrel 75 mg was found in a 100 count bottle of Metoprolol Succiante Extended-Release Tablets.
Contact the company
What happened, in plain English
Dr. Reddy's is recalling 100-mg Metoprolol Succinate Extended-Release Tablets because foreign Clopidogrel 75-mg tablets were found in some bottles. This could cause unintended medication interactions if taken. Read more at govinfonow.com/recall/40606-dr-reddy-s-metoprolol-tablets-recall-foreign-clopidogrel-tablets-found.
Source Summary by GovInfoNow · govinfonow.com/recall/40606-dr-reddy-s-metoprolol-tablets-recall-foreign-clopidogrel-tablets-found · Updated October 7, 2026 · FDA enforcement record: FDA #D-0727-2018
Cite this page
“Dr. Reddy's Metoprolol Tablets Recall: Foreign Clopidogrel Tablets Found.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/40606-dr-reddy-s-metoprolol-tablets-recall-foreign-clopidogrel-tablets-found. Based on FDA recall #D-0727-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0727-2018%22&limit=1).
Why it’s dangerous
Foreign Clopidogrel tablets were found in some bottles of Metoprolol. If taken, they could cause unintended medication interactions due to different blood-thinning effects.
Who’s affected
Prescription patients who received the recalled Metoprolol tablets from Dr. Reddy's. Those with specific medical conditions requiring precise medication timing are at higher risk.
How to tell if you have this one
Check for the product name 'Metoprolol Succinate Extended-Release Tablets, 100 mg, 100 tablets' with NDC 55111-468-01 and batch number C706254 from August 2019.
- Brand
Dr. Reddy's- Category
Drug
What to do — step by step
Check Your Medication
Look for the product name and batch number on the bottle label to confirm if it's recalled.
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 2.6 years 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-0727-2018 (April 23, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0727-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 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.