# China NMPA Product Recall - Infrared thermometer

Source: https://www.globalkeysolutions.net/records/china_product_recall/dongguan-haokang-electronics-technology-co-ltd/e11902a5-6126-48f8-abd1-22b79beef20f/
Source feed: China

> China NMPA product recall for Infrared thermometer by Dongguan Haokang Electronics Technology Co., Ltd. published August 31, 2021. Recall level: Level 3 Recall. The National Medical Products Administration (NMPA) published a notice on August 31, 2021, detailing

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Dongguan Zhenhai Electronics Technology Co., Ltd. voluntarily recalls infrared thermometers
- Company Name: Dongguan Haokang Electronics Technology Co., Ltd.
- Publication Date: 2021-08-31
- Product Name: Infrared thermometer
- Recall Level: Level 3 Recall
- Recall Reason: Measurement deviations were found during random inspections.
- Discovering Company: Dongguan Zhenhai Electronics Technology Co., Ltd.
- Manufacturing Company: Dongguan Haokang Electronics Technology Co., Ltd.
- Summary: The National Medical Products Administration (NMPA) published a notice on August 31, 2021, detailing a voluntary Class III recall initiated by Dongguan Zhenhai Electronics Technology Co., Ltd. This action was prompted by findings from random inspections, which revealed that the company's infrared thermometers exhibited measurement deviations, indicating a significant quality control issue.Operating under the regulatory framework of the NMPA and the Guangdong Provincial Drug Administration, Dongguan Zhenhai Electronics Technology Co., Ltd. has taken the required action of recalling its affected infrared thermometers, specifically those under Registration Certificate No.: 
粤械注 20152071173. The identified problem of inaccurate measurements presents a potential concern for users, necessitating this corrective measure to uphold product reliability and public health standards.Although specific inspection dates are not provided, the recall highlights the critical importance of continuous product quality oversight within the medical device sector. Further detailed information regarding the affected product models, specifications, and batch numbers is available in the "Medical Device Recall Event Report Form" referenced in the NMPA's announcement. This incident underscores both the regulatory body's role in monitoring product performance and manufacturers' responsibilities in proactively addressing quality and safety concerns.

Company: https://www.globalkeysolutions.net/companies/dongguan-haokang-electronics-technology-co-ltd/72dcc3aa-1f1e-40ff-995b-b99aaf6a8578/
