Data Foundry

Drug recalls 2019

ANASTROZOLE Tablets — Class II drug recall D-1440-2019

Terminated recall by Zydus Pharmaceuticals USA Inc, reported 2019-06-26, distributed nationwide. CGMP Deviations: Cross Contamination with other products due to CGMP cleaning failure.

Recall numberD-1440-2019
Product typeDrug
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmZydus Pharmaceuticals USA Inc, Pennington, NJ, United States
Recall initiated2019-05-06
Classified2019-07-01
Reported by FDA2019-06-26
Terminated2021-09-16
DistributedNationwide (US)
Reason classescgmp
NDC68382-0209, 68382-0209-06, 68382-0209-10
Lot numbersAPR-20, AUG-20, DEC-19, DEC-20, FEB-20, FEB-21, JAN-20, JAN-21, JUL-20, JUN-19, M706674, M706676, M707685, M711219, M711220, M711221, M711222, M711269, M801027, M801028, M801029, M801030, M802206, M805195, M805196, M805197, M805199, M805202, M805944, M805945, M805948, M805951, M805953, M805956, M805957, M805958, M805959, M812457, M812458, M812459 and 26 more

Product

ANASTROZOLE Tablets, 1 mg, Rx Only, 30-count bottle, Manufactured by: Cadila Healthcare Ltd. Ahmedabad, India. Distributed by: Zydus Pharmaceuticals (USA) Inc. Pennington, NJ 08534 NDC 68382-209-06

Reason for recall

CGMP Deviations: Cross Contamination with other products due to CGMP cleaning failure.

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-1440-2019. 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.