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

Source: https://www.globalkeysolutions.net/records/china_product_recall/yuxi-meichen-medical-supplies-co-ltd/0b825f81-3f17-4b51-9adc-1070e578e2d0/
Source feed: China

> China NMPA product recall for Disposable medical masks and medical surgical masks by Yuxi Meichen Medical Supplies Co., Ltd. published July 16, 2021. Recall level: Level 3 Recall. Yuxi Meichen Medical Supplies Co., Ltd. initiated a voluntary Class III recall of its disposable med

---

## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Yuxi Meichen Medical Supplies Co., Ltd. has voluntarily recalled disposable medical masks and medical surgical masks.
- Company Name: Yuxi Meichen Medical Supplies Co., Ltd.
- Publication Date: 2021-07-16
- Product Name: Disposable medical masks and medical surgical masks
- Recall Level: Level 3 Recall
- Recall Reason: The breaking strength of the mask straps does not meet the standard requirements.
- Discovering Company: Yuxi Meichen Medical Supplies Co., Ltd.
- Manufacturing Company: Yuxi Meichen Medical Supplies Co., Ltd.
- Summary: Yuxi Meichen Medical Supplies Co., Ltd. initiated a voluntary Class III recall of its disposable medical masks and surgical masks due to a critical quality issue. The recall, reported by the National Medical Products Administration (NMPA) and specifically sourced from the Yunnan Provincial Drug Administration website on July 16, 2021, addresses a deficiency where the breaking strength of the mask straps failed to meet required safety standards. The affected products include disposable medical masks (Registration No.: Dianxiezhuzhun 20202140032) and surgical masks (Registration No.: Dianxiezhuzhun 20202140062). This non-compliance poses a potential risk to users, as weakened straps could compromise the mask's ability to remain securely in place, thereby reducing its intended protective efficacy. Operating under the oversight of the NMPA, the company's proactive voluntary recall demonstrates adherence to regulatory expectations for addressing product safety concerns. The specific models, specifications, and batch information for the recalled devices are detailed in the "Medical Device Recall Event Report Form" attachments, emphasizing the structured process for such regulatory actions. This action underscores the importance of medical device manufacturers ensuring their products meet all stipulated quality and performance standards to safeguard public health.

Company: https://www.globalkeysolutions.net/companies/yuxi-meichen-medical-supplies-co-ltd/358a0450-8041-4c16-b3dd-5b06696d7fc6/
