RecallRadar

FDA Drug recall D-0649-2017

RIVASTIGMINE Tartrate Capsules, USP, 1.5 mg, 60-count bottle, Rx Only, Mfd

On 2017-04-12 the FDA classified a Class III recall of RIVASTIGMINE Tartrate Capsules, USP, 1.5 mg, 60-count bottle, Rx Only, Mfd by Dr Reddy S Laboratories, citing cross-contamination with other products -Related Substances test for Rivastigmine Tartrate Capsules USP, 1.5 mg showed a peak for Ranitidine.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0649-2017
ClassificationClass III
Statusterminated
Initiated2017-03-06
Published2017-04-12
Last updated2026-09-13 11:51 UTC
CompanyDr Reddy S Laboratories
DistributionUS

Product

RIVASTIGMINE Tartrate Capsules, USP, 1.5 mg, 60-count bottle, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Bachupally 500-900 India, NDC 55111-352-60

Reason

Cross-contamination with other products -Related Substances test for Rivastigmine Tartrate Capsules USP, 1.5 mg showed a peak for Ranitidine.

Identifiers

ndc55111-352-30
ndc55111-352-60
ndc55111-352-01
ndc55111-352-05
ndc55111-353-30
ndc55111-353-60
ndc55111-353-01
ndc55111-353-05
ndc55111-354-30
ndc55111-354-60
ndc55111-354-01
ndc55111-354-05
ndc55111-355-30
ndc55111-355-60
ndc55111-355-01
ndc55111-355-05
code_infoLot #C607323, Exp 10/18

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0649-2017%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.