Eribulin DRL (Eribulin Mesylate) - SAHPRA

Eribulin DRL (Eribulin Mesylate)

Eribulin DRL (Eribulin Mesylate)

Company name & Address:Registration numberBatch numberExpiry datePack sizeFirst Distribution dateRe-call ClassificationRecall date
Dr Reddys Laboratories (Pty) Ltd Block C, Woodmead North Office Park, 54 Maxwell Drive, Woodmead Sandton, Gauteng South Africa    57/26/0539    H260193     November 2027      2ml Vial      26 May 26    Class II Type C    22 September 2026

Brief description of the problem (reason for recall)

This recall is initiated due to extrapolated potential Out of Specification (OOS) assay result during routine long term stability testing. During Stability testing of different Eribulin batches, assay Out of Specification (OOS) results were recorded. Although the specific batch received in South Africa was not placed on stability, batch (H260193) will be recalled from the market as a precautionary measure.

Advice for health professionals and distributors:

Please immediately quarantine any units of the above-mentioned batch that you have in your possession and return via your normal distribution channel for full credit.

We apologize for any inconvenience and appreciate your assistance in this matter. Should you have any queries, please contact:

Dr Reddy’s Laboratories (Pty) Ltd

Tel: 011 3242100

e-mail: QA.SA@drreddys.com

Proposed action taken and its urgency: A SAHPRA approved recall letter was distributed to all distribution points, and the recall process was initiated.

Download latest version
Version: 1
Date Updated: 22/09/2026
File Type: www
Category: Product Recall
Unit: General ECTD & human medicines, Regulatory Compliance