# China NMPA Product Recall - Disposable medical masks

Source: https://www.keypedia.com/records/china_product_recall/suzhou-baixue-medical-equipment-co-ltd/0cfc3d08-2585-44ed-b675-72519087a754
Source feed: China

> China NMPA product recall for Disposable medical masks by Suzhou Baixue Medical Equipment Co., Ltd. published December 31, 2019. Recall level: Level 3 Recall. Suzhou Baixue Medical Device Co., Ltd. initiated a voluntary Class III recall of its disposable medi

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Suzhou Baixue Medical Device Co., Ltd. voluntarily recalls disposable medical masks.
- Company Name: Suzhou Baixue Medical Equipment Co., Ltd.
- Publication Date: 2019-12-31
- Product Name: Disposable medical masks
- Recall Level: Level 3 Recall
- Recall Reason: In the 2019 national medical device spot check, the mask's strap tension failed to meet the standard requirements.
- Discovering Company: Suzhou Baixue Medical Equipment Co., Ltd.
- Manufacturing Company: Suzhou Baixue Medical Equipment Co., Ltd.
- Summary: Suzhou Baixue Medical Device Co., Ltd. initiated a voluntary Class III recall of its disposable medical masks, identified by Registration Certificate Code Su Xie Zhu Zhun 20152641069. This action was officially reported on December 31, 2019, following findings from a 2019 national medical device spot check conducted under the oversight of the National Medical Products Administration (NMPA). The primary issue identified was the failure of the mask straps to meet established standard requirements. Such non-compliance poses a quality concern for medical devices intended for public use. The NMPA, as China's key regulatory authority for medical products, mandates stringent quality control for all medical devices sold within the country. In response to these findings, Suzhou Baixue Medical Device Co., Ltd. took the necessary corrective action by voluntarily recalling the affected batches of disposable masks. A Class III recall indicates that the use of, or exposure to, the non-conforming product is not likely to cause adverse health consequences. Detailed information concerning the specific models, specifications, and batches subject to this recall is documented in the "Medical Device Recall Event Report Form" issued by the company. This recall ensures that products not meeting safety and quality standards are removed from the market, upholding consumer safety and regulatory compliance.

Company: https://www.keypedia.com/companies/suzhou-baixue-medical-equipment-co-ltd/67f822df-d738-41b9-9f22-c495d8f1515c