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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

Presence of Foreign Substance: A product complaint was received for a defective tablet with an embedded foreign object observed in a bottle.

🇺🇸 FDA recall #D-0878-2018DrugDr. Reddy's Laboratories, Inc. ›
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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.
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Source Page by GovInfoNow · govinfonow.com/recall/40507-dr-reddy-s-laboratories-inc-recalls-atorvastatin-calcium-tablets-80 · Recall date May 30, 2018 · FDA enforcement record: FDA #D-0878-2018

Cite this page

“Dr. Reddy's Laboratories, Inc. recalls Atorvastatin Calcium Tablets, 80 mg*, 90-count bottles, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam.” GovInfoNow, recall dated May 30, 2018. https://govinfonow.com/recall/40507-dr-reddy-s-laboratories-inc-recalls-atorvastatin-calcium-tablets-80. Based on FDA recall #D-0878-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0878-2018%22&limit=1).

How to tell if you have this one

  • Brand
    Dr. Reddy's Laboratories, Inc.
  • Product
    Atorvastatin Calcium Tablets, 80 mg*, 90-count bottles, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam
  • Category
    Drug
Take action

Contact Dr. Reddy's Laboratories, Inc.

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

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

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 Laboratories, Inc..

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.
  • 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