RecallRadar

FDA Drug recall D-0726-2022

Atorvstatin Calcium Tablets, USP 80 mg*, 90 Tablets, Rx Only, Mrd

On 2022-04-06 the FDA classified a Class III recall of Atorvstatin Calcium Tablets, USP 80 mg*, 90 Tablets, Rx Only, Mrd by Dr Reddy S Laboratories, citing failed Impurities/Degradation Specifications: Out of Specification results for related substance.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0726-2022
ClassificationClass III
Statusterminated
Initiated2022-03-16
Published2022-04-06
Last updated2026-09-13 11:52 UTC
CompanyDr Reddy S Laboratories
DistributionUS

Product

Atorvstatin Calcium Tablets, USP 80 mg*, 90 Tablets, Rx Only, Mrd. By: Dr. Reddy's Laboratories Limited, Srikakulam - 532 409, INDIA, NDC 55111-124-90

Reason

Failed Impurities/Degradation Specifications: Out of Specification results for related substance.

Identifiers

ndc55111-124-30
ndc55111-124-60
ndc55111-124-90
ndc55111-124-05
code_infoLot: T000707, T000756, T000758, T000759, Exp 03/2022; T2100600, T2101075, Exp. 1/2023; T2102802, Exp. 07/2023

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0726-2022%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.