RecallRadar

FDA Drug recall D-0886-2018

Atorvastatin Calcium Tablets, 10 mg*, 90-count bottle, Rx Only, Mfd

On 2018-06-27 the FDA classified a Class III recall of Atorvastatin Calcium Tablets, 10 mg*, 90-count bottle, Rx Only, Mfd by Dr Reddy S Laboratories, citing failed Impurities/Degradation Specifications.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0886-2018
ClassificationClass III
Statusterminated
Initiated2018-06-12
Published2018-06-27
Last updated2026-09-13 11:52 UTC
CompanyDr Reddy S Laboratories
DistributionUS

Product

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

Reason

Failed Impurities/Degradation Specifications

Identifiers

ndc55111-121-30
ndc55111-121-60
ndc55111-121-90
ndc55111-121-05
ndc55111-121-10
ndc55111-122-30
ndc55111-122-60
ndc55111-122-90
ndc55111-122-05
ndc55111-122-10
ndc55111-123-30
ndc55111-123-60
ndc55111-123-90
ndc55111-123-05
ndc55111-123-10
code_infoLot #: T600327, Exp 07/18; T700213, T700215, Exp 04/19

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-0886-2018%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.