Another batch of feminine hygiene solution was discovered to violate quality regulations.

On September 10, the Drug Administration of Vietnam (Ministry of Health) issued a decision to suspend circulation and recall nationwide two batches of cosmetics due to poor quality and violations of labeling regulations. Among them, there is a feminine hygiene solution product.

Nationwide recall of Ori Women Pluss feminine hygiene solution

Specifically, according to the official dispatch of Nghe An Department of Health , the test results showed that the batch of Ori Women Pluss Feminine Hygiene Solution (box of 1 bottle of 120ml, batch number: 160324, Manufacturing date: March 16, 2024, Expiry date: March 16, 2027) produced by SJK Pharmaceutical and Cosmetic Biotechnology Company Limited (Hanoi), Bao Minh Chau Herbal Medicine and Medical Equipment Joint Stock Company (Hai Phong) is responsible for bringing to the market, did not meet the standards for microbial limit indicators.

The test sample was taken at the counter of Que Phong Pharmaceutical Branch ( Nghe An ). The Drug Administration requested to suspend circulation, recall and destroy the entire batch of this product.

Provincial and municipal health departments are responsible for notifying businesses and users to immediately stop consuming the product, monitor recalls and handle violations.

The two companies involved must urgently organize the recall and destruction and report the results to the department before October 4.

In addition, the Center for Drug, Cosmetic and Food Testing ( Can Tho Department of Health) also reported that the product batch LD Perfume Oil (box of 1 bottle of 12ml, batch number: LD043979, Expiry date: 36 months after opening) brought to the market by LD Group Trading and Production Company Limited (Can Tho) did not meet the quality standards in terms of sensory indicators and violated labeling regulations (lack of information on production date and batch number).

The Drug Administration Department requested the suspension of circulation and nationwide recall of this product batch. LD Group Company must recall, destroy, and review the labels of other batches to correct similar errors and report to the department before September 19.

The Drug Administration of Vietnam requests local health departments to closely monitor the recall and destruction of businesses; and at the same time, check compliance with regulations on cosmetics management in production and business activities. In case of detecting violations, they must be strictly handled according to current regulations.

Consumers are advised to carefully check product information, immediately stop using cosmetic batches that have been suspended from circulation and promptly report to authorities when discovering products suspected of being unsafe.

The company voluntarily recalled 4 CELL29 products

In addition, the Drug Administration Department also announced the withdrawal of 4 cosmetic product declaration receipt numbers requested by NEXTGEN INTERNATIONAL JSC (HCMC) to stop business, including:

1. CELL29 REPASIVE BLEMISH BALM

2. CELL29 LUONLIGHT POTENCY CREAM

3. CELL29 ILLUNA-EX BOOSTER

4. CELL29 GEN-3 TONER

All four products above are manufactured by HWCOSCOCO CO., LTD (Korea) and licensed for circulation by the Drug Administration of Vietnam in February 2025.

WILLOW

Source: https://tuoitre.vn/lai-phat-hien-lo-dung-dich-ve-sinh-phu-nu-vi-pham-quy-dinh-ve-chat-luong-2025091014542769.htm