# China NMPA Product Recall - Low-frequency therapy device

Source: https://www.globalkeysolutions.net/records/china_product_recall/guangzhou-yalo-beauty-equipment-co-ltd/7e0e1189-daaf-432c-b173-bf3927156ad2/
Source feed: China

> China NMPA product recall for Low-frequency therapy device by GUANGZHOU YALO BEAUTY EQUIPMENT CO., LTD published January 18, 2022. Recall level: Level 2 Recall. The National Medical Products Administration (NMPA) announced on January 18, 2022, a Class II volunt

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Guangzhou Aofang Beauty Equipment Co., Ltd. voluntarily recalls low-frequency therapy devices.
- Company Name: GUANGZHOU YALO BEAUTY EQUIPMENT CO., LTD
- Publication Date: 2022-01-18
- Product Name: Low-frequency therapy device
- Recall Level: Level 2 Recall
- Discovering Company: Guangzhou Aofang Beauty Equipment Co., Ltd.
- Manufacturing Company: GUANGZHOU YALO BEAUTY EQUIPMENT CO., LTD
- Summary: The National Medical Products Administration (NMPA) announced on January 18, 2022, a Class II voluntary recall initiated by Guangzhou Aofang Beauty Equipment Co., Ltd. This action concerns the company's low-frequency therapy devices. The specific reasons prompting this recall, along with detailed information regarding the affected product models, specifications, and batch numbers, are not elaborated within this announcement. Instead, these critical details are referenced as being available in a separate "Medical Device Report Form" and an attached "Medical Device Recall Event Report Form.pdf." Under the oversight of the NMPA, this voluntary recall signifies a commitment by Guangzhou Aofang Beauty Equipment Co., Ltd. to address potential issues with its medical devices. While the precise nature of the concern leading to the recall remains undisclosed in this public notice, a Class II recall typically indicates a situation where the use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote. The company is taking responsibility by recalling these devices from the market. This regulatory framework ensures that medical device manufacturers comply with safety and quality standards, protecting public health. Consumers and healthcare providers are advised to refer to the comprehensive recall documentation for specific instructions and further details regarding the required actions for affected products.

Company: https://www.globalkeysolutions.net/companies/guangzhou-yalo-beauty-equipment-co-ltd/a5a3f9f4-95d7-4e93-901e-1c86337888bd/
