# China NMPA Product Recall - Disposable medical masks (non-sterile)

Source: https://www.globalkeysolutions.net/records/china_product_recall/guangdong-baihe-medical-technology-co-ltd/cd438940-10cd-4da9-9bcc-8a5b5b4ff932/
Source feed: China

> China NMPA product recall for Disposable medical masks (non-sterile) by Guangdong Baihe Medical Technology Co., Ltd published January 04, 2021. Recall level: Level 3 Recall. On January 4, 2021, the National Medical Products Administration (NMPA) issued a notice regarding a 

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Guangdong Tianqi Medical Technology Co., Ltd. has voluntarily recalled its disposable medical masks (non-sterile).
- Company Name: Guangdong Baihe Medical Technology Co., Ltd
- Publication Date: 2021-01-04
- Product Name: Disposable medical masks (non-sterile)
- Recall Level: Level 3 Recall
- Recall Reason: The ventilation resistance does not meet the technical requirements of YY/T0969-2013.
- Discovering Company: Guangdong Tianqi Medical Technology Co., Ltd.
- Manufacturing Company: Guangdong Baihe Medical Technology Co., Ltd
- Summary: On January 4, 2021, the National Medical Products Administration (NMPA) issued a notice regarding a voluntary product recall initiated by Guangdong Tianqi Medical Technology Co., Ltd. The company proactively recalled its disposable medical masks (non-sterile), identified under Registration Certificate No. "".The decision to recall stemmed from the company's discovery that a sampled batch of their masks failed to meet critical technical requirements. Specifically, the ventilation resistance of the product was found to be non-compliant with the standards outlined in YY/T0969-2013, a key regulatory specification for medical masks. This issue indicates a potential deviation from established safety and performance criteria, which could impact the product's intended protective function.Guangdong Tianqi Medical Technology Co., Ltd. classified this as a Level III recall, indicating that the use of or exposure to the product is not likely to cause adverse health consequences. The company's immediate action was to initiate a voluntary recall to address the identified quality deficiency. This regulatory action, overseen by the Guangdong Provincial Drug Administration, underscores the importance of manufacturers adhering to product specifications and ensuring consumer safety in the medical device sector.

Company: https://www.globalkeysolutions.net/companies/guangdong-baihe-medical-technology-co-ltd/79d2e901-9843-48f0-8311-ef9f3c32b884/