# China NMPA Product Recall - Ultrasound diagnostic system, ultrasound diagnostic instrument

Source: https://www.globalkeysolutions.net/records/china_product_recall/shenzhen-baisheng-medical-technology-co-ltd/9c9d7f5c-3376-4226-bbc9-ef4e4f074265/
Source feed: China

> China NMPA product recall for Ultrasound diagnostic system, ultrasound diagnostic instrument by Shenzhen Baisheng Medical Technology Co., Ltd. published January 04, 2021. Recall level: . Shenzhen Baisheng Medical Technology Co., Ltd. initiated a voluntary recall of specific ultrasonic d

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Shenzhen Baisheng Medical Technology Co., Ltd. has initiated a voluntary recall of its ultrasound diagnostic systems and ultrasound diagnostic instruments.
- Company Name: Shenzhen Baisheng Medical Technology Co., Ltd.
- Publication Date: 2021-01-04
- Product Name: Ultrasound diagnostic system, ultrasound diagnostic instrument
- Recall Reason: The power adapter assembly has reliability issues; failure to operate it according to the user manual will affect its use.
- Discovering Company: Shenzhen Baisheng Medical Technology Co., Ltd.
- Manufacturing Company: Shenzhen Baisheng Medical Technology Co., Ltd.
- Summary: Shenzhen Baisheng Medical Technology Co., Ltd. initiated a voluntary recall of specific ultrasonic diagnostic systems and instruments, as announced by the National Medical Products Administration (NMPA) on January 4, 2021. This action was prompted by a report from the company's power adapter supplier, detailing component reliability issues with adapters used in some portable ultrasound products. These issues could potentially affect product functionality if users do not adhere strictly to the instructions outlined in the user manual.

The recall encompasses an ultrasound diagnostic system (Registration Certificate No.: 粤械注准20162230080) and an ultrasound diagnostic instrument (Registration Certificate No.: 国械注进20202060249). This voluntary measure falls under the regulatory purview of the NMPA and reflects the company's commitment to product safety. Further comprehensive details, including the recall level, specific product models, specifications, and affected batches, are provided in the accompanying "Medical Device Recall Event Report Form," available to guide stakeholders and users through the recall process.

Company: https://www.globalkeysolutions.net/companies/shenzhen-baisheng-medical-technology-co-ltd/9f979272-96d8-46f2-bdb2-1a3ba0587cea/