Zydus Pharmaceuticals USA Inc recalls Carvedilol Tablets, USP, 3.125 mg, 500-count bottle, Rx Only, Manufactured by: Cadila Healthcare Ltd., India;
Zydus Pharmaceuticals recalls 3.125mg Carvedilol tablets due to foreign tablets found in some bottles. Customers should check their bottles for light yellow fragments.
Lower-risk recall
Presence of Foreign Tablets/Capsules: Customer complaint for a small, solid, light yellow substance, identified as a fragmented tablet of another drug product, found mixed with tablets in a bottle of Carvedilol tablets 3.125mg.
Contact the company & request your remedy
What happened, in plain English
Zydus Pharmaceuticals is recalling 3.125 mg Carvedilol tablets because customers reported finding small light yellow fragments of another drug in the bottles. This could lead to accidental ingestion of an unintended medication. Read more at govinfonow.com/recall/38892-zydus-carvedilol-tablets-recall-foreign-tablets-found-in-bottle.
Source Summary by GovInfoNow · govinfonow.com/recall/38892-zydus-carvedilol-tablets-recall-foreign-tablets-found-in-bottle · Updated October 5, 2026 · FDA enforcement record: FDA #D-1242-2019
Cite this page
“Zydus Carvedilol Tablets Recall: Foreign Tablets Found in Bottle.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/38892-zydus-carvedilol-tablets-recall-foreign-tablets-found-in-bottle. Based on FDA recall #D-1242-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1242-2019%22&limit=1).
Why it’s dangerous
Customers reported finding small, light yellow fragments of another drug product mixed with Carvedilol tablets in the bottle. This means someone might accidentally take the foreign tablets instead of the intended medication.
Who’s affected
People with a prescription for Carvedilol tablets who received this specific bottle from Zydus Pharmaceuticals. Those who have the bottle with the NDC 68382-092-05 lot number Z803518 are most at risk.
How to tell if you have this one
Check your Carvedilol tablets for small light yellow fragments. The affected bottles have NDC 68382-092-05 and lot number Z803518, manufactured by Cadila Healthcare Ltd. in India.
- Brand
Zydus Pharmaceuticals- Category
Drug
What to do — step by step
Check Your Bottles
Look for small light yellow fragments inside the Carvedilol tablets bottle.
Questions people ask
Is this recall dangerous?
The recall is for foreign tablets found in some bottles, but the risk is low as no injuries have been reported.
How do I know if I have the recalled product?
Check for the NDC 68382-092-05 and lot number Z803518 on the bottle.
What should I do if I find foreign tablets?
Discard the bottle and contact your doctor or pharmacist for advice.
Contact Zydus Pharmaceuticals
We’ve drafted a message you can send Zydus Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-1242-2019 — Zydus Pharmaceuticals Zydus Pharmaceuticals Hello, I own a Zydus Pharmaceuticals that is covered by recall D-1242-2019 from Zydus 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-1242-2019 (April 22, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1242-2019 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.