# China NMPA Product Recall - Medical disposable protective clothing

Source: https://www.globalkeysolutions.net/records/china_product_recall/guangzhou-boxue-biotechnology-co-ltd/8864f80f-65a7-4fa3-9808-babc7386d6e4/
Source feed: China

> China NMPA product recall for Medical disposable protective clothing by Guangzhou Boxue Biotechnology Co., Ltd published August 01, 2022. Recall level: . Guangzhou Beogene Biotechnology Co., Ltd. initiated a voluntary product recall on August 1, 2022, fo

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Guangzhou Beogene Biotechnology Co., Ltd. voluntarily recalls disposable medical protective clothing.
- Company Name: Guangzhou Boxue Biotechnology Co., Ltd
- Publication Date: 2022-08-01
- Product Name: Medical disposable protective clothing
- Recall Reason: The zipper in the appearance cannot be
- Discovering Company: Guangzhou Beogene Biotechnology Co., Ltd.
- Manufacturing Company: Guangzhou Boxue Biotechnology Co., Ltd
- Summary: Guangzhou Beogene Biotechnology Co., Ltd. initiated a voluntary product recall on August 1, 2022, for its disposable medical protective suits. The recall specifically targets suits from batch number 2020120101, which bears Registration Certificate No.: 粤械注准20202140532. This action was taken following a random inspection that identified a critical defect: a faulty zipper on one 175mm specification disposable medical protective suit. This quality issue compromises the protective integrity of the medical device. The recall is being conducted under the oversight of the National Medical Products Administration (NMPA), indicating compliance with national medical device regulations in China. While specific inspection dates are not provided, the issue was discovered during a routine random quality check. As a required action, Guangzhou Beogene Biotechnology Co., Ltd. has voluntarily recalled the affected products from the market. Further detailed information regarding the recall level, specific product models, and specifications is available in the associated "Medical Device Recall Event Report Form." This proactive measure aims to ensure patient and user safety by removing non-conforming products from circulation, upholding the manufacturer's responsibility for product quality.

Company: https://www.globalkeysolutions.net/companies/guangzhou-boxue-biotechnology-co-ltd/4f986b14-7757-4b68-8e97-40cd3280c9e7/