D-1287-2022 Class II Terminated

Recalled by Dr. Reddy's Laboratories, Inc. — Princeton, NJ

FDA drug recall D-1287-2022 was initiated by Dr. Reddy's Laboratories, Inc. on Jul 13, 2022 and is designated Class II. Reason for recall: FAILED DISSOLUTION SPECIFICATIONS The recall status is terminated (terminated Dec 6, 2023). Affected quantity: 2,892 cartons.

Recall Details

Product Type
Drugs
Report Date
Aug 3, 2022
Initiation Date
Jul 13, 2022
Termination Date
Dec 6, 2023
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
2,892 cartons

Product Description

Lansoprazole Delayed-Release Orally Disintegrating Tablets, 15 mg, 100-count blisters per carton, 10 Packs of 10 Tablets Each, Rx Only, Distributed by: Dr. Reddy's Laboratories, Inc., Princeton, NJ 08540, Made in India, blister barcode 4359856079, NDC 43598-560-78

Reason for Recall

FAILED DISSOLUTION SPECIFICATIONS

Distribution Pattern

Nationwide in the USA

Code Information

Lot T2100514, Exp 01/2023

Source

Dataset
openFDA drug recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for D-1287-2022
openFDA file date
Oct 23, 2026
Loaded by RegDataLab
Oct 25, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.