On September 10, the Drug Administration of Vietnam (Ministry of Health) issued a document announcing the suspension of circulation, recall and destruction of the batch of cosmetic products Ori Women Pluss Women's Hygiene Solution - Box of 1 bottle of 120 ml due to not meeting quality standards on microorganistic limitations.
According to the document, the product has the receipt number of the 052/24/CBMP-HN declaration form; batch number 160324; production date of March 16, 2024; expiration date of March 16, 2027. The unit responsible for bringing the product to the market is Bao Minh Chau Herbal and Medical Equipment Joint Stock Company (address: 392 Nguyen Luong Bang, Phu Lien Ward, Hai Phong City), manufactured at SJK Pharmaceutical Biotechnology and Cosmetics Company Limited (address: Lot CN2, Phu Nghia Industrial Park, Phu Nghia Commune, Hanoi City).
The test sample was taken by the Center for Testing Drugs, Cosmetics, and Food - Nghe An Department of Health at Que Phong Pharmaceutical Branch counter (Tien Phong commune, Nghe An province). Test results showed that the product was not of good quality and had to be recalled nationwide.
The Drug Administration of Vietnam requests the Department of Health of provinces and cities to notify cosmetic businesses and users in the area to immediately stop trading and using the above product batch and return it to the supplier. At the same time, localities must organize the recovery, destruction and supervision of this process, strictly handling violations.
Bao Minh Chau Company and SJK Company are responsible for sending recall notices to distribution and use locations; receiving and recalling all defective products; and at the same time, proceeding with destruction in accordance with regulations. The two companies must report the results of the recovery and destruction to the Drug Administration before October 4, 2025.
The Hai Phong City Department of Health and the Hanoi City Department of Health are assigned to supervise the recovery, destruction as well as inspect the production and trading of cosmetics of the two related enterprises. The results of the inspection and supervision must be reported to the Department of Drug Administration before October 19, 2025.
On the same day, the Drug Administration Department also issued a document suspending the circulation, recall and destruction nationwide of the LD Perfume Oil cosmetic batch - Box of 1 bottle of 12ml due to poor quality and violation of regulations on labeling.
The product batch has batch number SX: LD043979, validity period of 36 months after opening the lid. The unit responsible for bringing the product to the market is LD Group Trading and Production Company Limited (current address: 325E, KV1, Cai Rang ward, Can Tho city). Notably, the product box does not have the date of manufacture, and the bottle does not record the production lot number.
The test sample was taken directly by the Center for Drug, Cosmetic and Food Testing - Can Tho City Department of Health at LD Group Company for quality control. The results showed that the test sample did not meet sensory targets and did not meet regulations on labeling, and had to be recalled.
The Drug Administration of Vietnam requests the Departments of Health of provinces and cities to notify businesses and users to immediately stop the circulation of the above product, and at the same time organize the recovery, destruction, supervision of the handling process and strictly handle violations.
LD Group Trading and Production Company Limited sent a notice of revocation to the distribution and use establishments of the product; received the returned product and organized the destruction of the entire batch of violating products.
Report the results of recovery and destruction to the Department of Drug Administration before October 4, 2025.
Check the labels of other product lots. If similar errors are detected, they must be urgently recalled and reported to the Department before September 19, 2025. The enterprise will be fully responsible before the law if the report is dishonest.
The Department of Health of Can Tho City is assigned to supervise LD Group Company in recalling and destroying substandard products; at the same time, inspect compliance with regulations on cosmetic management and punish violations if any. The results of the inspection and supervision must be reported to the Department of Drug Administration before October 19, 2025.
