# China NMPA Product Recall - Electronic thermometer

Source: https://www.globalkeysolutions.net/records/china_product_recall/guangzhou-aixinda-electronics-co-ltd/ff21c292-3590-4e12-9a1a-549edbc52d8d/
Source feed: China

> China NMPA product recall for Electronic thermometer by Guangzhou Aixinda Electronics Co., Ltd. published November 11, 2020. Recall level: Level 3 Recall. The National Medical Products Administration (NMPA) published an announcement on November 11, 2020, 

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Guangzhou Aixinda Electronics Co., Ltd. voluntarily recalls electronic thermometers
- Company Name: Guangzhou Aixinda Electronics Co., Ltd.
- Publication Date: 2020-11-11
- Product Name: Electronic thermometer
- Recall Level: Level 3 Recall
- Discovering Company: Guangzhou Aixinda Electronics Co., Ltd.
- Manufacturing Company: Guangzhou Aixinda Electronics Co., Ltd.
- Summary: The National Medical Products Administration (NMPA) published an announcement on November 11, 2020, detailing a voluntary product recall initiated by Guangzhou Aixinda Electronics Co., Ltd. The company is recalling certain models of its electronic thermometers, an action categorized as a Level III recall. This classification typically indicates that while a product issue exists, its use or exposure is unlikely to result in significant adverse health consequences. The announcement from the NMPA serves as an official public record of this recall. While specific details concerning the exact models, technical specifications, and affected production batches of the electronic thermometers are not provided in this public notification, the document refers to a more comprehensive "Medical Device Notice" and an attached "Recall Incident Report Form.pdf" for this information. This framework ensures that detailed product-specific data is available to relevant parties and the public through official channels. The voluntary nature of the recall indicates that the company identified a potential issue and took proactive steps to address it under the regulatory oversight of the NMPA, which is the primary authority for medical device supervision. The required action for the company is to execute this Level III recall, which involves identifying and removing the affected products from the market to ensure consumer safety and compliance with regulatory standards.

Company: https://www.globalkeysolutions.net/companies/guangzhou-aixinda-electronics-co-ltd/9b763c2d-75a5-49eb-a65f-214cdb675c65/