# China NMPA Product Recall - Arm-type electronic blood pressure monitor

Source: https://www.globalkeysolutions.net/records/china_product_recall/guangzhou-aixinda-electronics-co-ltd/4c58701a-f424-4d3e-a5bd-9faca6aecedf
Source feed: China

> China NMPA product recall for Arm-type electronic blood pressure monitor by Guangzhou Aixinda Electronics Co., Ltd. published July 18, 2022. Recall level: Level 3 Recall. Guangzhou Aixinda Electronics Co., Ltd. has initiated a voluntary Class III recall of its arm-type e

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Guangzhou Aixinda Electronics Co., Ltd. voluntarily recalls arm-type electronic blood pressure monitors
- Company Name: Guangzhou Aixinda Electronics Co., Ltd.
- Publication Date: 2022-07-18
- Product Name: Arm-type electronic blood pressure monitor
- Recall Level: Level 3 Recall
- Recall Reason: An arm-type electronic blood pressure monitor with production batch number 20200615 was found to be non-compliant with standards during a random inspection.
- Discovering Company: Guangzhou Aixinda Electronics Co., Ltd.
- Manufacturing Company: Guangzhou Aixinda Electronics Co., Ltd.
- Summary: Guangzhou Aixinda Electronics Co., Ltd. has initiated a voluntary Class III recall of its arm-type electronic blood pressure monitors. This action follows a random inspection that identified a specific production batch (number 20200615) as non-compliant with established standards. The recall details, including affected product models and the precise nature of the non-compliance, are further outlined in the company's Medical Device Recall Event Report Form. This regulatory oversight and subsequent recall align with the framework governed by the National Medical Products Administration (NMPA) and the Guangdong Provincial Drug Administration, ensuring product safety and quality within the medical device sector. Guangzhou Aixinda Electronics Co., Ltd. is responsible for implementing the necessary steps to address the non-compliance and manage the recall process, with consumers and healthcare providers advised to refer to the official recall documentation for guidance on required actions.

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