Data Foundry

Drug recalls 2015

Rivastigmine Tartrate Capsules — Class II drug recall D-1325-2015

Terminated recall by Dr. Reddy's Laboratories, Inc., reported 2015-08-19, distributed nationwide. Failed Dissolution Specifications

Recall numberD-1325-2015
Product typeDrug
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmDr. Reddy's Laboratories, Inc., Princeton, NJ, United States
Recall initiated2015-08-03
Classified2015-08-11
Reported by FDA2015-08-19
Terminated2017-03-24
DistributedNationwide (US)
Quantity2,952 bottles
Reason classesspecification failure
NDC55111-0352, 55111-0352-01, 55111-0352-05, 55111-0352-30, 55111-0352-60, 55111-0353, 55111-0353-01, 55111-0353-05, 55111-0353-30, 55111-0353-60, 55111-0354, 55111-0354-01, 55111-0354-05, 55111-0354-30, 55111-0354-60, 55111-0355, 55111-0355-01, 55111-0355-05, 55111-0355-30, 55111-0355-60
Lot numbersC501342
Expiration dates2017-01

Product

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

Reason for recall

Failed Dissolution Specifications

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1325-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.