The Drug Administration of Vietnam (Ministry of Health) has just requested the suspension of circulation, recall and destruction nationwide of the Tabame Pro postpartum shower and bath product batch due to not meeting quality standards for microbial limiting indicators.
According to the Drug Administration of Vietnam, the recalled product batch is Xông tắm gội cho bà mẹ sau sinh (brand Tabame Pro), box size 1 bottle 400 ml, Receipt number Cosmetic Product Declaration Form 23/25/CBMP-QN, batch number 300326, production date March 30, 2026, expiry date March 30, 2029.
The product is produced by Anh Minh Pharmaceutical Trading and Service Co., Ltd. responsible for bringing it to the market and Xanh DT Pharmaceutical Co., Ltd.
The test results of the Ho Chi Minh City Center for Drug, Cosmetic and Food Testing showed that the product sample taken at the warehouse of Van Phuoc General Hospital Co., Ltd. (Ho Chi Minh City) did not meet quality standards for microbial limiting indicators.
Based on the test results, the Drug Administration of Vietnam requested the suspension of circulation and nationwide recall of the above batch of products.
The Drug Administration of Vietnam requests Departments of Health of provinces and cities to notify establishments trading and using cosmetics to immediately stop trading and using violating product batches and return them to supply establishments; and at the same time strengthen inspection and supervision of the recall and strict handling of violating organizations and individuals according to regulations.
For related businesses, the Drug Administration of Vietnam requests Anh Minh Pharmaceutical Trading and Service Co., Ltd. and Xanh DT Pharmaceutical Co., Ltd. to urgently notify the entire distribution system, receive returned products, organize the recall and destruction of the entire batch of products that do not meet quality regulations.
The two enterprises must complete the recall, destruction and submit a report to the Drug Administration of Vietnam before August 20, 2026.
In addition, the Ho Chi Minh City Department of Health and the Quang Ninh Provincial Department of Health are assigned to supervise the recall and destruction process; and at the same time inspect the compliance with legal regulations on cosmetics management in the production and business activities of related enterprises. The results of inspection and handling must be reported to the Drug Administration of Vietnam before September 5, 2026.
