CLASS III Drug recall · Reported 23 Jun 2021 · FDA Enforcement Report

Atorvastatin Calcium Tablets, USP 10 mg recalled

Dr. Reddy's Laboratories is recalling Atorvastatin Calcium Tablets, USP 10 mg, distributed nationwide in the US. The recall was initiated on 4 Jun 2021 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesLot #: C905064, C905065, Exp. Date 07/2021
NDC55111-121, 55111-122, 55111-123
UPC0355111123903
Quantity recalled5984 bottles

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0629-2021
FDA event ID
88041
Recalling firm
Dr. Reddy's Laboratories, Princeton, NJ
Manufacturer
Dr. Reddy's Laboratories Limited
Classification
Class III
Status
Terminated
Recall initiated
4 Jun 2021
FDA classified
11 Jun 2021
Reported
23 Jun 2021
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Potency & Assay

Timeline

4 Jun 2021Recall initiated by company
11 Jun 2021Classified by FDA+7 days
23 Jun 2021Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Failed Impurities/Degradation Specifications: due to presence of ATV cyclo IP and FP impurities

Potency and specification recalls happen when a batch tests outside its approved limits for strength, purity or dissolution, which can mean the dose delivered is higher or lower than labelled.

Product as listed by the FDA

Atorvastatin Calcium Tablets, USP 10 mg, 500-count bottles, Rx Only, Dr. Reddy's Mfd. By: Dr. Reddy's Laboratories Limited, Bachupally, 500-090 India, NDC 55111-121-05.

Where it was distributed

Nationwide within the United States

Nationwide

Questions about this recall

Why was it recalled?

Failed Impurities/Degradation Specifications: due to presence of ATV cyclo IP and FP impurities

Which lots are affected?

Lot #: C905064, C905065, Exp. Date 07/2021

Where was it sold?

Nationwide within the United States

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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