# China NMPA Product Recall - Disposable face masks (emergency COVID-19 response products) (non-sterile)

Source: https://www.globalkeysolutions.net/records/china_product_recall/guangdong-yifang-pharmaceutical-co-ltd/a020e1bb-1a65-4dbb-aafa-c062869c601f/
Source feed: China

> China NMPA product recall for Disposable face masks (emergency COVID-19 response products) (non-sterile) by Guangdong Yifang Pharmaceutical Co., Ltd published May 19, 2022. Recall level: Level 3 Recall. Guangdong Yidetang Pharmaceutical Co., Ltd. has initiated a voluntary recall of its disposable non-s

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Guangdong Yidetang Pharmaceutical Co., Ltd. has voluntarily recalled its disposable masks (emergency epidemic prevention products) (non-sterile).
- Company Name: Guangdong Yifang Pharmaceutical Co., Ltd
- Publication Date: 2022-05-19
- Product Name: Disposable face masks (emergency COVID-19 response products) (non-sterile)
- Recall Level: Level 3 Recall
- Discovering Company: Guangdong Yidetang Pharmaceutical Co., Ltd.
- Manufacturing Company: Guangdong Yifang Pharmaceutical Co., Ltd
- Summary: Guangdong Yidetang Pharmaceutical Co., Ltd. has initiated a voluntary recall of its disposable non-sterile masks, specifically those marketed as emergency products for epidemic prevention. This significant regulatory action was publicly announced on May 19, 2022, under the oversight of the National Medical Products Administration (NMPA) and the Guangdong Provincial Drug Administration. The recall is categorized as Level III, a classification used when exposure to the product is unlikely to cause adverse health consequences, yet a recall is deemed necessary to address specific deficiencies. Although the precise details concerning the product issues leading to this voluntary recall are not elaborated in the public notice, the company has taken proactive measures to ensure product quality and consumer safety. Comprehensive information, including the specific models affected and the full scope of the recall event, is documented in the "Medical Device Recall Event Report Form." This document serves as the official record outlining the company's assessment and the specific actions required to address the identified concerns. The NMPA, as the primary regulatory authority, oversees such recalls to maintain the integrity and safety of medical devices within the market, reinforcing public trust in these essential products.

Company: https://www.globalkeysolutions.net/companies/guangdong-yifang-pharmaceutical-co-ltd/07846ca9-3cec-469c-8361-754173210343/