# China NMPA Product Recall - Disposable medical masks and surgical caps

Source: https://www.globalkeysolutions.net/records/china_product_recall/wujiang-yicheng-medical-equipment-co-ltd/ae805a1f-0e29-4e07-b7dc-1c44a9823db0/
Source feed: China

> China NMPA product recall for Disposable medical masks and surgical caps by Wujiang Yicheng Medical Equipment Co., Ltd. published December 31, 2019. Recall level: Level 3 Recall. Wujiang Yicheng Medical Device Co., Ltd. has initiated a voluntary Level III recall for its disposab

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Wujiang Yicheng Medical Device Co., Ltd. has voluntarily recalled disposable medical masks and surgical caps.
- Company Name: Wujiang Yicheng Medical Equipment Co., Ltd.
- Publication Date: 2019-12-31
- Product Name: Disposable medical masks and surgical caps
- Recall Level: Level 3 Recall
- Recall Reason: In the 2019 national medical device spot check, the masks failed to meet the requirements for bacterial filtration rate.
- Discovering Company: Wujiang Yicheng Medical Equipment Co., Ltd.
- Manufacturing Company: Wujiang Yicheng Medical Equipment Co., Ltd.
- Summary: Wujiang Yicheng Medical Device Co., Ltd. has initiated a voluntary Level III recall for its disposable medical masks and surgical caps. This action, reported on December 31, 2019, follows critical findings from a 2019 national medical device spot check overseen by the National Medical Products Administration (NMPA). The primary issue identified was that the company's disposable medical masks, registered under certificate code Su Xie Zhu Zhun 20162640249, failed to meet the required bacterial filtration rate standards. This particular deficiency is significant for medical masks, as their effectiveness in preventing the spread of airborne bacteria directly depends on robust filtration capabilities. The NMPA's regulatory framework mandates strict adherence to such performance criteria to safeguard public health and ensure the reliability of medical products. The company's voluntary recall demonstrates its response to these findings, with detailed information on the specific models, specifications, and affected batches provided in the 'Medical Device Recall Event Report Form.' This incident highlights the continuous need for rigorous quality assurance and compliance with national medical device standards to maintain product integrity and user safety in healthcare environments.

Company: https://www.globalkeysolutions.net/companies/wujiang-yicheng-medical-equipment-co-ltd/852d22cb-71ae-41e6-9c7f-61839cd77b5a/