# China NMPA Product Recall - Disposable medical masks

Source: https://www.globalkeysolutions.net/records/china_product_recall/sichuan-hengming-technology-development-co-ltd/9c6246a7-b779-441c-80e0-9fdea5de6906/
Source feed: China

> China NMPA product recall for Disposable medical masks by Sichuan Hengming Technology Development Co., Ltd. published December 05, 2019. Recall level: Level 3 Recall. Sichuan Hengming Technology Development Co., Ltd. initiated a voluntary Class III recall of its disp

---

## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Sichuan Hengming Technology Development Co., Ltd. has voluntarily recalled disposable medical masks.
- Company Name: Sichuan Hengming Technology Development Co., Ltd.
- Publication Date: 2019-12-05
- Product Name: Disposable medical masks
- Recall Level: Level 3 Recall
- Recall Reason: The product in question failed a provincial-level supervision and spot check in Sichuan Province in 2019. The tested sample failed to meet the product technical requirements for "the breaking strength at the connection between the mask strap and the mask body".
- Discovering Company: Sichuan Hengming Technology Development Co., Ltd.
- Manufacturing Company: Sichuan Hengming Technology Development Co., Ltd.
- Summary: Sichuan Hengming Technology Development Co., Ltd. initiated a voluntary Class III recall of its disposable medical masks on December 5, 2019. This action followed findings from the 2019 Sichuan Provincial Supervision and Spot Check, which identified a significant quality deviation in the product. Specifically, the tested samples failed to meet the specified technical requirements for the "breaking strength at the connection between the mask strap and the mask body." This deficiency indicates a potential risk regarding the integrity and secure fit of the masks during use, which is critical for their intended protective function. The National Medical Products Administration (NMPA) oversees such regulatory actions, ensuring compliance with product safety standards. The Class III recall designation signifies that the product defect is unlikely to cause adverse health consequences, but still warrants removal from the market to maintain quality and safety expectations. The company voluntarily undertook this recall to address the non-compliance identified by the provincial regulatory inspection. Further details regarding the specific batches and affected products were to be outlined in a separate Medical Device Recall Event Report Form. This recall underscores the importance of continuous quality control and adherence to technical specifications for medical devices to safeguard public health.

Company: https://www.globalkeysolutions.net/companies/sichuan-hengming-technology-development-co-ltd/b29a8422-614a-4992-8185-0e2620a6639e/