# China NMPA Product Recall - Medical isolation shoe covers

Source: https://www.globalkeysolutions.net/records/china_product_recall/guangzhou-boxue-biotechnology-co-ltd/db5553b5-a195-4ba4-9087-ee8d74a85605/
Source feed: China

> China NMPA product recall for Medical isolation shoe covers by Guangzhou Boxue Biotechnology Co., Ltd published August 01, 2022. Recall level: Level 3 Recall. Guangzhou Beogene Biotechnology Co., Ltd. has initiated a voluntary recall of its medical isolation 

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Guangzhou Beogene Biotechnology Co., Ltd. voluntarily recalls its medical isolation shoe covers.
- Company Name: Guangzhou Boxue Biotechnology Co., Ltd
- Publication Date: 2022-08-01
- Product Name: Medical isolation shoe covers
- Recall Level: Level 3 Recall
- Recall Reason: Non-compliance with medical device instruction manual label management requirements
- Discovering Company: Guangzhou Beogene Biotechnology Co., Ltd.
- Manufacturing Company: Guangzhou Boxue Biotechnology Co., Ltd
- Summary: Guangzhou Beogene Biotechnology Co., Ltd. has initiated a voluntary recall of its medical isolation shoe covers due to non-compliance with medical device instruction label management requirements. The recall, published by the National Medical Products Administration (NMPA) on August 1, 2022, specifically targets products with production batch number 2022052501, which were sold on May 26, 2022. The issue centers on the product's labeling, which failed to meet the established standards for medical devices, as overseen by the NMPA and the Guangdong Provincial Drug Administration. This regulatory framework mandates strict adherence to labeling guidelines to ensure product safety and proper usage information for consumers and healthcare professionals. In response to this violation, Guangzhou Beogene Biotechnology Co., Ltd. has decided to implement a Level III recall. This action requires the company to remove the affected medical isolation shoe covers from distribution to rectify the labeling deficiency. The "Medical Device Recall Event Report Form" provides further details on the specific models, specifications, and batches involved in this recall. This voluntary action underscores the company's responsibility to address product compliance and maintain public safety standards.

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