# China NMPA Product Recall - Disposable sterile masks

Source: https://www.globalkeysolutions.net/records/china_product_recall/harbin-taigu-industrial-co-ltd/0a00f6f2-6389-4a03-8fd5-964522d1edaf/
Source feed: China

> China NMPA product recall for Disposable sterile masks by Harbin Taigu Industrial Co., Ltd. published July 15, 2019. Recall level: Level III. On July 15, 2019, the National Medical Products Administration (NMPA) of China publicized a voluntar

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Harbin Taigu Industrial Co., Ltd. voluntarily recalls "disposable sterile masks"
- Company Name: Harbin Taigu Industrial Co., Ltd.
- Publication Date: 2019-07-15
- Product Name: Disposable sterile masks
- Recall Level: Level III
- Recall Reason: In the 2019 national medical device spot check, the "bacterial filtration efficiency" item did not meet the standard requirements, posing a potential risk.
- Discovering Company: Harbin Taigu Industrial Co., Ltd.
- Manufacturing Company: Harbin Taigu Industrial Co., Ltd.
- Summary: On July 15, 2019, the National Medical Products Administration (NMPA) of China publicized a voluntary Level III recall initiated by Harbin Taigu Industrial Co., Ltd. The recall concerns specific batches of their "Disposable Sterile Masks," particularly those with production batch number 20190315. This action was prompted by a national medical device spot check conducted in 2019, which revealed that these masks failed to meet the critical standard for bacterial filtration efficiency. A deficiency in bacterial filtration efficiency means the masks may not adequately protect against airborne bacteria, posing a potential health risk to users. The NMPA, as China's primary medical product regulator, oversees such surveillance and enforcement activities to ensure the safety and efficacy of medical devices available to the public. Harbin Taigu Industrial Co., Ltd. proactively took action by recalling the affected products, demonstrating their commitment to addressing product quality issues. This Level III classification indicates that while the products may be in violation of NMPA regulations, the likelihood of serious adverse health consequences is generally low, though the potential for risk remains. The recall details, including specific models and specifications, are further elaborated in the "Medical Device Voluntary Recall Event Report Form." This event underscores the rigorous regulatory oversight by the NMPA in maintaining product quality and public trust within the medical device sector.

Company: https://www.globalkeysolutions.net/companies/harbin-taigu-industrial-co-ltd/b4e076b0-9b5c-49f6-a153-766143cec75b/