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Drug recall · FDA · Published May 30, 2018

Dr. Reddy's Laboratories, Inc. recalls Atorvastatin Calcium Tablets, 80 mg*, 90-count bottles, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam

Dr. Reddy's recalls 80mg Atorvastatin tablets due to foreign objects in some bottles. Consumers should check NDC 55111-124-90 for affected lots. No remedy specified in official notice.

🇺🇸 FDA recall #D-0878-2018DrugDr. Reddy's ›
Take action

Contact the company & request your remedy

Recalling firmDr. Reddy's Laboratories, Inc.107 College Rd E, N/A · Princeton, NJ 08540-6623
No email on file for this recall — reach the company by phone or its official page instead.No email on file — write to the address above instead.
✎ GovInfoNow plain-language explainer

What happened, in plain English

Dr. Reddy's is recalling 80mg Atorvastatin Calcium tablets that may contain foreign objects. This could cause injury if the object is ingested or causes choking. The recall affects prescription bottles with specific NDC and lot numbers. Read more at govinfonow.com/recall/40507-dr-reddy-s-atorvastatin-80mg-tablets-recall-foreign-object-hazard.

Source Summary by GovInfoNow · govinfonow.com/recall/40507-dr-reddy-s-atorvastatin-80mg-tablets-recall-foreign-object-hazard · Updated October 7, 2026 · FDA enforcement record: FDA #D-0878-2018

Cite this page

“Dr. Reddy's Atorvastatin 80mg Tablets Recall: Foreign Object Hazard.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/40507-dr-reddy-s-atorvastatin-80mg-tablets-recall-foreign-object-hazard. Based on FDA recall #D-0878-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0878-2018%22&limit=1).

Why it’s dangerous

Foreign objects in the tablets could be ingested, potentially causing choking or injury. The hazard is not described as causing serious injury in normal use, so the risk is low.

Who’s affected

Prescription users of Atorvastatin 80mg tablets with NDC 55111-124-90 and lot number T800064. People who have taken these tablets since the manufacturing date (Dec 2019) may be affected.

How to tell if you have this one

Check for NDC 55111-124-90 and lot number T800064 on the bottle. The product was manufactured in India by Dr. Reddy's Laboratories Limited, Srikakulam.

  • Brand
    Dr. Reddy's
  • Product
    Atorvastatin Calcium Tablets, 80 mg*, 90-count bottles, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for NDC 55111-124-90 and lot number T800064 on the bottle label.

✎ GovInfoNow

Questions people ask

Is there a remedy for this recall?

The official recall notice does not specify any remedy.

What should I do if I have the recalled product?

Check the product details to see if it matches the recalled lot number. If it does, contact Dr. Reddy's for further instructions.

How can I tell if my Atorvastatin tablets are affected?

Look for NDC 55111-124-90 and lot number T800064 on the bottle. The product was manufactured in India by Dr. Reddy's Laboratories Limited, Srikakulam.

Take action

Contact Dr. Reddy's

We’ve drafted a message you can send Dr. Reddy's to request your refund or repair — edit it as you like.

Subject: Recall D-0878-2018 — Dr. Reddy's Atorvastatin Calcium Tablets, 80 mg*, 90-count bottles, Rx Only, Mfd. By: Dr. Reddy's L

Hello,

I own a Atorvastatin Calcium Tablets, 80 mg*, 90-count bottles, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam that is covered by recall D-0878-2018 from Dr. Reddy's.

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-0878-2018 (May 30, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0878-2018 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA