Dr. Reddy's Laboratories, Inc. recalls Atorvastatin Calcium Tablets, USP 10 mg*, Rx Only, 500 count bottle, Mfd By: Dr. Reddy's Laboratories Limited,
Dr. Reddy's recalls 10mg Atorvastatin tablets due to impurities that may affect drug safety. Learn if your product is affected and what to do.
Lower-risk recall
Failed Impurities -Degradation Specifications:due to presence of ATV cyclo IP and FP impurities
Contact the company & request your remedy
What happened, in plain English
Dr. Reddy's is recalling 10mg Atorvastatin Calcium tablets because they contain impurities that could affect drug safety. This recall affects prescription-only bottles sold in the U.S. from specific manufacturers and lots. Read more at govinfonow.com/recall/36156-dr-reddy-s-atorvastatin-tablets-recall-impurities-risk-drug-safety.
Source Summary by GovInfoNow · govinfonow.com/recall/36156-dr-reddy-s-atorvastatin-tablets-recall-impurities-risk-drug-safety · Updated October 4, 2026 · FDA enforcement record: FDA #D-0599-2021
Cite this page
“Dr. Reddy's Atorvastatin Tablets Recall: Impurities Risk Drug Safety.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/36156-dr-reddy-s-atorvastatin-tablets-recall-impurities-risk-drug-safety. Based on FDA recall #D-0599-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0599-2021%22&limit=1).
Why it’s dangerous
The tablets contain impurities called ATV cyclo IP and FP that may affect drug safety. These impurities could potentially alter the medication's effectiveness or safety profile, though the exact risk level is not specified in the recall.
Who’s affected
Prescription users of Dr. Reddy's 10mg Atorvastatin tablets in the U.S. who received the specific lot number C905063 (expiring July 2021) are affected. Patients taking this medication should check if their bottle matches the recall details.
How to tell if you have this one
Check for the product name 'Atorvastatin Calcium Tablets, USP 10 mg', prescription-only, 500-count bottle, manufactured by Dr. Reddy's Laboratories Limited in Bachupally, India. Look for the lot number C905063 with an expiration date of July 2021.
- Brand
Dr. Reddy's- Category
Drug
What to do — step by step
Check Product Details
Identify if your bottle matches the recall: 10mg Atorvastatin tablets, prescription-only, 500-count, manufactured by Dr. Reddy's Laboratories Limited in Bachupally, India, lot C905063 (expiring July 2021).
Questions people ask
Is this product safe to use?
The recall states the tablets contain impurities that may affect drug safety, but the exact risk level is not specified. Consult your doctor for personalized advice.
What should I do if I have this product?
The recall does not specify a remedy, so check with your doctor or pharmacist to determine if you need to take action.
How can I confirm if my product is recalled?
Look for the product name 'Atorvastatin Calcium Tablets, USP 10 mg', prescription-only, 500-count bottle, manufactured by Dr. Reddy's Laboratories Limited in Bachupally, India, with lot number C905063 (expiring July 2021).
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-0599-2021 — Dr. Reddy's Dr. Reddy's Hello, I own a Dr. Reddy's that is covered by recall D-0599-2021 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-0599-2021 (May 4, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0599-2021 to see it in context.
- Plain-language summary written by qwen3:4b on October 4, 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.