# China NMPA Product Recall - Disposable medical masks

Source: https://www.globalkeysolutions.net/records/china_product_recall/anhui-yiwei-medical-supplies-co-ltd/47eb2b5f-0e9e-4072-a400-b181ceeb3f6b/
Source feed: China

> China NMPA product recall for Disposable medical masks by Anhui Yiwei Medical Supplies Co., Ltd. published July 22, 2022. Recall level: Level 3 Recall. Anhui Yimeijian Medical Supplies Co., Ltd. initiated a voluntary Class III recall of its disposable 

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Anhui Yimeijian Medical Supplies Co., Ltd. has voluntarily recalled disposable medical masks.
- Company Name: Anhui Yiwei Medical Supplies Co., Ltd.
- Publication Date: 2022-07-22
- Product Name: Disposable medical masks
- Recall Level: Level 3 Recall
- Recall Reason: Failed market sampling inspection
- Discovering Company: Anhui Yimeijian Medical Supplies Co., Ltd.
- Manufacturing Company: Anhui Yiwei Medical Supplies Co., Ltd.
- Summary: Anhui Yimeijian Medical Supplies Co., Ltd. initiated a voluntary Class III recall of its disposable medical masks, specifically those from batch number 20210202. This action was taken following the failure of these masks in a market sampling inspection. The recall was publicly reported by the National Medical Products Administration (NMPA) on July 22, 2022, referencing information from the Anhui Provincial Drug Administration. The primary issue identified was that a specific batch of disposable medical masks did not meet required quality standards during routine market surveillance. While the exact nature of the failure is not detailed in the provided document, the initiation of a recall indicates a significant deviation from product specifications or safety requirements. The company, Anhui Yimeijian Medical Supplies Co., Ltd., is responsible for the manufacturing and quality assurance of these medical devices. Under the oversight of the NMPA and its provincial counterpart, the Anhui Provincial Drug Administration, the company is undertaking corrective actions by removing the non-compliant products from distribution. A Class III recall signifies that the use of or exposure to a violative product is not likely to cause adverse health consequences. Detailed information regarding the product models, specifications, and affected batch sizes is available in the "Medical Device Recall Event Report Form," which presumably outlines the scope and procedures for the recall. This incident underscores the importance of continuous quality monitoring and regulatory compliance for medical device manufacturers to ensure public health and safety.

Company: https://www.globalkeysolutions.net/companies/anhui-yiwei-medical-supplies-co-ltd/1d68da68-550d-426f-af3c-b65df65873bd/