Dr. Reddy's Laboratories, Inc. recalls Atorvastatin Calcium Tablets, 40 mg*, packaged as a) 90-count bottle (NDC 55111-123-90 and b) 500-count bottle (NDC
Dr. Reddy's recalls 40mg Atorvastatin Calcium tablets due to failed impurities and degradation. Rx-only bottles with specific NDCs and lots may be affected. Consumers should contact the manufacturer for details.
Recall notice
Failed Impurities/Degradation Specifications
Contact the company & request your remedy
What happened, in plain English
Dr. Reddy's is recalling 40mg Atorvastatin Calcium tablets that may have failed impurities or degradation. This could pose a risk to users taking the medication, though the exact danger is not specified in the recall notice. Read more at govinfonow.com/recall/40455-dr-reddy-s-atorvastatin-40mg-tablets-recall-failed-impurities-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/40455-dr-reddy-s-atorvastatin-40mg-tablets-recall-failed-impurities-risk · Updated October 7, 2026 · FDA enforcement record: FDA #D-0888-2018
Cite this page
“Dr. Reddy's Atorvastatin 40mg Tablets Recall: Failed Impurities Risk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/40455-dr-reddy-s-atorvastatin-40mg-tablets-recall-failed-impurities-risk. Based on FDA recall #D-0888-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0888-2018%22&limit=1).
Why it’s dangerous
The tablets may have failed impurities or degradation specifications, which could affect their safety and effectiveness. However, the recall does not specify how this could cause harm or what the exact risk level is.
Who’s affected
People who have been prescribed these specific 40mg Atorvastatin tablets by a doctor. Those with the listed NDC numbers and expiration dates are most at risk.
How to tell if you have this one
Check for the 90-count or 500-count bottles with NDC numbers 55111-123-90 or 55111-123-05. The lot numbers and expiration dates listed in the recall (e.g., T600392, Exp 08/18) indicate which batches are affected.
- 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 in the USA and Puerto Rico- 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-0886-2018 | Atorvastatin Calcium Tablets, 10 mg*, 90-count bottle, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam - 532 409 INDIA, NDC 55111-121-90; Lot #: T600327, Exp 07/18; T700213, T700215, Exp 04/19 | 55,126 bottles |
| D-0887-2018 | Atorvastatin Calcium Tablets, 20 mg*, 90-count bottle, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam - 532 409 INDIA, NDC 55111-122-90; Lot #: T600328, Exp 07/18; T700214, T700216, Exp 04/19 | 44,894 bottles |
| D-0888-2018 | Atorvastatin Calcium Tablets, 40 mg*, packaged as a) 90-count bottle (NDC 55111-123-90 and b) 500-count bottle (NDC 55111-123-05), Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam - 532 409 INDIA; Lot #: a) T600392, T600384, T600353, Exp 08/18; T600427, Exp 09/18; T600435, Exp 10/18; T600492, Exp 11/18; T700006, T700014, T700033, T700035, T700036 12/18; b) T600407, Exp 09/18 | 130,081 bottles |
What to do — step by step
Check Product Details
Identify the NDC number and expiration date on your bottle to see if it matches the recalled lots listed in the notice.
Questions people ask
Why is this product being recalled?
The recall is for failed impurities or degradation specifications, but the exact risk to users is not clearly described in the notice.
What should I do if I have this product?
The recall does not specify a remedy, so contact Dr. Reddy's Laboratories directly for further instructions.
Are there specific batches that are affected?
Yes, specific lot numbers and expiration dates are listed in the recall (e.g., T600392, Exp 08/18).
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-0888-2018 — Dr. Reddy's Dr. Reddy's Hello, I own a Dr. Reddy's that is covered by recall D-0888-2018 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-0888-2018 (June 12, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0888-2018 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.