# China NMPA Product Recall - Medical surgical masks, disposable medical masks

Source: https://www.globalkeysolutions.net/records/china_product_recall/anhui-jiangzhong-gaobang-pharmaceutical-co-ltd/75c4f741-b416-4fd1-bc2d-d2137f942585/
Source feed: China

> China NMPA product recall for Medical surgical masks, disposable medical masks by Anhui Jiangzhong Gaobang Pharmaceutical Co., Ltd. published September 30, 2021. Recall level: Level 3 Recall. Anhui Jiangzhong Gaobang Pharmaceutical Co., Ltd. initiated a voluntary Class III recall of specific

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Anhui Jiangzhong Gaobang Pharmaceutical Co., Ltd. voluntarily recalls medical devices.
- Company Name: Anhui Jiangzhong Gaobang Pharmaceutical Co., Ltd.
- Publication Date: 2021-09-30
- Product Name: Medical surgical masks, disposable medical masks
- Recall Level: Level 3 Recall
- Recall Reason: Ear loop tensile strength test failed
- Discovering Company: Anhui Jiangzhong Gaobang Pharmaceutical Co., Ltd.
- Manufacturing Company: Anhui Jiangzhong Gaobang Pharmaceutical Co., Ltd.
- Summary: Anhui Jiangzhong Gaobang Pharmaceutical Co., Ltd. initiated a voluntary Class III recall of specific medical device products following a provincial regulatory spot check. The recall, publicly reported on September 30, 2021, by the National Medical Products Administration (NMPA) and originating from the Anhui Provincial Drug Administration, pertains to medical surgical masks with batch numbers 20210109 and 20210114, and disposable medical masks with batch number 20210207. The primary issue identified was a failure in the ear loop tensile strength test for these affected batches. This deficiency indicates a potential quality concern that could compromise the intended function and safety of the masks. In response to these findings, Anhui Jiangzhong Gaobang Pharmaceutical Co., Ltd. is taking proactive measures to remove the non-compliant products from the domestic market. A Class III recall typically signifies a situation where the use of, or exposure to, a violative product is not likely to cause adverse health consequences. The company has submitted a "Medical Device Recall Event Report Form" and a "Gaobang Medical Device Voluntary Recall Report" to document the details and execution of this recall. This action underscores the company's commitment to product quality and patient safety under the oversight of national and provincial regulatory bodies.

Company: https://www.globalkeysolutions.net/companies/anhui-jiangzhong-gaobang-pharmaceutical-co-ltd/08b3b5e4-0d4e-41e2-bb4e-5d7f3130dd29/