Print version of this report
Type of Product Medicine
TGA Recall Reference RC-2017-RN-00756-1
Product Name/Description Amlodipine Sandoz 5mg tablets

Batch Number: GT3446

Expiry: Oct-2019

Pack size: 30

AUST R: 124578
Recall Action Level Consumer
Recall Action Classification Class II
Recall Action Commencement Date 9/06/2017
Responsible Entity Sandoz Pty Ltd
Reason/Issue Sandoz has initiated a Recall of affected Amlodipine Sandoz 5mg tablets due to a possibility of missing blisters in the cartons. Please note there is no quality or safety issue with the tablets themselves.
Recall Action Recall
Recall Action Instructions Sandoz is conducting a consumer level Recall of affected units only from one batch. For further information please see: https://www.tga.gov.au/alert/amlodipine-sandoz-tablets .


This action has been reviewed and is considered complete in accordance with the requirements of the URPTG.
Contact Information 02 8584 3337 – Sandoz Quality Assurance
1800 726 369 – Sandoz Customer Service/Medical Information