# China NMPA Product Recall - Medical surgical masks

Source: https://www.globalkeysolutions.net/records/china_product_recall/hebei-baota-medical-equipment-co-ltd/53af93e7-3e8d-4b74-bd9d-8c2643fbbac7/
Source feed: China

> China NMPA product recall for Medical surgical masks by Hebei Baota Medical Equipment Co., Ltd. published March 29, 2021. Recall level: Level 3 Recall. On March 29, 2021, the National Medical Products Administration (NMPA) announced a voluntary Level I

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Hebei Baota Medical Equipment Co., Ltd.'s voluntary recall notice for medical surgical masks
- Company Name: Hebei Baota Medical Equipment Co., Ltd.
- Publication Date: 2021-03-29
- Product Name: Medical surgical masks
- Recall Level: Level 3 Recall
- Recall Reason: Packaging does not meet regulations
- Discovering Company: Hebei Baota Medical Equipment Co., Ltd.
- Manufacturing Company: Hebei Baota Medical Equipment Co., Ltd.
- Summary: On March 29, 2021, the National Medical Products Administration (NMPA) announced a voluntary Level III recall initiated by Hebei Baota Medical Device Co., Ltd. This recall specifically targets the company's medical surgical masks, identified by Registration No.: 冀械注准20172640240.

The primary reason for this recall is the non-compliance of the product's packaging with established regulations. This issue was self-identified and reported by Hebei Baota Medical Device Co., Ltd. to the Hebei Provincial Drug Administration. While the specific nature of the packaging non-compliance is not detailed in the announcement, the action highlights the critical importance of adhering to regulatory standards for medical device packaging to ensure product integrity and safety.

Operating under the regulatory framework of the NMPA, this voluntary recall mechanism ensures that products failing to meet designated quality or safety criteria are systematically removed from the market. A Level III recall classification typically indicates that the use of the non-compliant product is unlikely to result in adverse health consequences. Hebei Baota Medical Device Co., Ltd. has submitted a 'Medical Device Recall Event Report Form,' which outlines the specific models, specifications, and batch numbers of the affected products. This proactive measure demonstrates the company's commitment to product quality and consumer safety in collaboration with regulatory authorities.

Company: https://www.globalkeysolutions.net/companies/hebei-baota-medical-equipment-co-ltd/edf4e578-6913-412b-9fbf-04511f0be106/