# China NMPA Product Recall - Disposable medical masks

Source: https://www.globalkeysolutions.net/records/china_product_recall/yangzhou-xinglan-pharmaceutical-technology-co-ltd/8301708e-be28-4942-8d7d-caba7cd5b0fa
Source feed: China

> China NMPA product recall for Disposable medical masks by Yangzhou Xinglan Pharmaceutical Technology Co., Ltd published August 30, 2021. Recall level: Level 3. Anhui Xingye Pharmaceutical Technology Co., Ltd. initiated a voluntary Class III recall of its dispo

---

## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Anhui Xingye Pharmaceutical Technology Co., Ltd. has voluntarily recalled disposable medical masks.
- Company Name: Yangzhou Xinglan Pharmaceutical Technology Co., Ltd
- Publication Date: 2021-08-30
- Product Name: Disposable medical masks
- Recall Level: Level 3
- Recall Reason: Failed the random inspection
- Discovering Company: Anhui Xingye Pharmaceutical Technology Co., Ltd.
- Manufacturing Company: Yangzhou Xinglan Pharmaceutical Technology Co., Ltd
- Summary: Anhui Xingye Pharmaceutical Technology Co., Ltd. initiated a voluntary Class III recall of its disposable medical masks, specifically those from batch number 20200624. This action was announced on August 30, 2021, following the failure of these masks during a random quality inspection. The National Medical Products Administration (NMPA), the regulatory body responsible for overseeing medical products, publicized this recall through its official website. The recall became necessary after the specified batch of disposable medical masks did not meet established quality standards during routine random inspections. While the exact nature of the failure is not detailed in the public notice, the company's decision to voluntarily recall the product indicates a recognition of a quality deficiency that warrants removal from the market. A Level III recall signifies that exposure to the product is not likely to cause adverse health consequences. Anhui Xingye Pharmaceutical Technology Co., Ltd. is taking the required action to remove the non-compliant products from distribution and use. Further details regarding the specific models, specifications, and additional batches involved, if any, are documented in the "Medical Device Recall Event Report Form" attached to the official NMPA notice. This proactive measure by the company, under the oversight of the NMPA, underscores the commitment to product safety and regulatory compliance in the medical device sector. The public is directed to the NMPA website for further information and contact details.

Company: https://www.globalkeysolutions.net/companies/yangzhou-xinglan-pharmaceutical-technology-co-ltd/2513306c-feba-4b07-aea5-3d8e0e5d181d