# China NMPA Product Recall - Disposable medical surgical masks

Source: https://www.globalkeysolutions.net/records/china_product_recall/guizhou-junjiang-industrial-co-ltd/ebf23e2a-2de3-4656-8dbb-6c82086f2d72/
Source feed: China

> China NMPA product recall for Disposable medical surgical masks by Guizhou Junjiang Industrial Co., Ltd. published April 02, 2021. Recall level: Level 3 Recall. Guizhou Junjiang Industrial Co., Ltd. initiated a voluntary recall of its disposable medical surgica

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Guizhou Junjiang Industrial Co., Ltd. has voluntarily recalled its disposable medical surgical masks.
- Company Name: Guizhou Junjiang Industrial Co., Ltd.
- Publication Date: 2021-04-02
- Product Name: Disposable medical surgical masks
- Recall Level: Level 3 Recall
- Recall Reason: The product's mask strap connection point's breaking strength and sterility do not meet the "Technical Requirements for Disposable Medical Surgical Masks".
- Discovering Company: Guizhou Junjiang Industrial Co., Ltd.
- Manufacturing Company: Guizhou Junjiang Industrial Co., Ltd.
- Summary: Guizhou Junjiang Industrial Co., Ltd. initiated a voluntary recall of its disposable medical surgical masks (Registration Certificate No.: 黔械注准20172640019) following a public report on April 2, 2021. The recall, overseen by the National Medical Products Administration (NMPA) and the Guizhou Provincial Drug Administration, addresses a significant quality non-compliance. The primary issue identified is a failure to meet established technical requirements at the connection point between the mask strap and the mask itself. This defect poses a risk to the product's integrity and could compromise its effectiveness and user safety. In response to this deficiency, Guizhou Junjiang Industrial Co., Ltd. proactively took action to retrieve the affected products from the market. The NMPA has classified this as a Level III recall, which signifies that the use of or exposure to the non-compliant product is not anticipated to cause adverse health consequences. However, it still mandates the removal of specific product batches to uphold quality standards and mitigate potential risks. Details regarding the affected batch numbers and product specifications are documented in the "Medical Device Recall Report Form," an attachment to the official NMPA notice. This action underscores the company's commitment to regulatory compliance and product safety under the NMPA framework.

Company: https://www.globalkeysolutions.net/companies/guizhou-junjiang-industrial-co-ltd/f43cabab-b6eb-4b75-84fb-30587357059f/