According to the Hanoi Department of Health, the gietinol tablets in the intestines of Rabewell-20, circulation registration number: VN-13640-11, batch number: ME23A40, manufactured by The Madras Pharmaceuticals Company (India) on January 18, 2026.
This product is imported by A My Pharmaceutical Company Limited and distributed by My Anh Trading and Service Joint Stock Company. The reason for the recall is that the drug does not meet the quality requirements of the luongodiction target.
The Hanoi Department of Health requires My Anh Trading and Service Trading Joint Stock Company to thoroughly recall the Rabewell-20 intestinal sales vien (Rabeprazole Sodium); submit a recall report and recall dossier according to regulations.
In addition, public health facilities under the industry, non-public health facilities, drug businesses, and drug retail facilities in the area urgently review and recall drug lots that do not meet the above quality standards.
The health departments of districts, towns and cities notify establishments in the management area; conduct inspections and supervise the implementation of the recall of establishments (if any).
