Dr. Reddy's Laboratories, Inc. recalls Atorvastatin Calcium Tablets 10 mg, a) 90 count and b) 500 count bottles, Rx only, Mfd by: Dr. Reddy's Laboratories,
Dr. Reddy's recalls 10mg Atorvastatin Calcium tablets with impurities detected. Affected lots from March 2018 and May 2018. Stop using if you have these specific bottles.
Recall notice
Failed Impurities/Degradations Specifications; out-of-specification results observed for Total Degradation Impurities during stability
Contact the company & request your remedy
What happened, in plain English
Dr. Reddy's is recalling 10mg Atorvastatin Calcium tablets that tested with impurities. This could pose a risk to your health if taken. The recall affects specific batches made in India between March and May 2018. Read more at govinfonow.com/recall/40896-dr-reddy-s-atorvastatin-10mg-tablets-recall-impurities-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/40896-dr-reddy-s-atorvastatin-10mg-tablets-recall-impurities-risk · Updated October 7, 2026 · FDA enforcement record: FDA #D-0418-2018
Cite this page
“Dr. Reddy's Atorvastatin 10mg Tablets Recall: Impurities Risk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/40896-dr-reddy-s-atorvastatin-10mg-tablets-recall-impurities-risk. Based on FDA recall #D-0418-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0418-2018%22&limit=1).
Why it’s dangerous
The tablets failed quality tests for impurities and degradation. This means the medication might not be safe for use and could cause health issues if taken. The problem was found during stability testing.
Who’s affected
People who have prescription Atorvastatin Calcium 10mg tablets from Dr. Reddy's in India, specifically the 90-count and 500-count bottles with the listed lot numbers. Those taking this medication are most at risk.
How to tell if you have this one
Check for the brand Dr. Reddy's, product name Atorvastatin Calcium 10mg, and the specific lot numbers: T600125 (March 2018) or T600201/T600248 (May 2018). The product comes in 90-count or 500-count bottles.
- Brand
Dr. Reddy's- Category
Drug
All 3 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class III- Status
Terminated- Distribution
Nationwide- NDC
55111-121-30, 55111-121-60, 55111-121-90, 55111-121-05, 55111-121-10, 55111-122-30, 55111-122-60, 55111-122-90, 55111-122-05, 55111-122-10, 55111-123-30, 55111-123-60, 55111-123-90, 55111-123-05, 55111-123-10
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-0418-2018 | Atorvastatin Calcium Tablets 10 mg, a) 90 count and b) 500 count bottles, Rx only, Mfd by: Dr. Reddy's Laboratories, Ltd., Srikakulam, INDIA --- NDC 55111-121-05; Lot numbers: a) T600125, 3/2018; T600201, T600248 5/2018, b) T600125, 3/2018; T600201, and T600248, 5/2018 | a) 34,125; b) 3,540 bottles |
| D-0419-2018 | Atorvastatin Calcium Tablets 20 mg, a) 90 count and b) 500 count bottles, Rx only, Mfd by: Dr. Reddy's Laboratories, Ltd., Srikakulam, INDIA --- NDC 55111-122-05; Lot numbers: a) T600126, 3/2018; T600202 and T600247 5/2018, b) T600126, 3/2018; T600202, and T600247, 5/2018 | a) 28,941 and b) 2,928 bottles |
| D-0420-2018 | Atorvastatin Calcium Tablets 40 mg, 90 count bottles, Rx only, Mfd by: Dr. Reddy's Laboratories, Ltd., Srikakulam, INDIA --- NDC 55111-123-05; Lot number: T600279, 6/2018 | 12,579 bottles |
What to do — step by step
Check Your Product
Look for the lot numbers T600125 (March 2018) or T600201/T600248 (May 2018) on the bottle.
Questions people ask
Why is this medication being recalled?
The tablets failed quality tests for impurities and degradation, which could pose a health risk.
What should I do if I have these tablets?
The recall record does not specify a remedy, so you should contact your doctor or pharmacist for advice.
Are there specific batches that are affected?
Yes, the affected batches have lot numbers T600125 (March 2018) or T600201/T600248 (May 2018).
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-0418-2018 — Dr. Reddy's Dr. Reddy's Hello, I own a Dr. Reddy's that is covered by recall D-0418-2018 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-0418-2018 (January 29, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0418-2018 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.