# China NMPA Product Recall - Infrared thermometer

Source: https://www.globalkeysolutions.net/records/china_product_recall/beile-guangzhou-intelligent-information-technology-co-ltd/80bb5e24-1dfa-44ea-bb4f-d1f272b11c8b/
Source feed: China

> China NMPA product recall for Infrared thermometer by Beile (Guangzhou) Intelligent Information Technology Co., Ltd. published October 21, 2021. Recall level: Level 3 Recall. Beile (Guangzhou) Intelligent Information Technology Co., Ltd. has initiated a voluntary Level III r

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Beile (Guangzhou) Intelligent Information Technology Co., Ltd. voluntarily recalls infrared thermometers
- Company Name: Beile (Guangzhou) Intelligent Information Technology Co., Ltd.
- Publication Date: 2021-10-21
- Product Name: Infrared thermometer
- Recall Level: Level 3 Recall
- Recall Reason: Random inspections revealed that the products did not meet the required standards.
- Discovering Company: Beile (Guangzhou) Intelligent Information Technology Co., Ltd.
- Manufacturing Company: Beile (Guangzhou) Intelligent Information Technology Co., Ltd.
- Summary: Beile (Guangzhou) Intelligent Information Technology Co., Ltd. has initiated a voluntary Level III recall of its infrared thermometers, specifically targeting production batch number 210120B10. This action, published on October 21, 2021, by the National Medical Products Administration (NMPA), through the Guangdong Provincial Drug Administration, follows findings from routine random inspections. The primary issue identified was that the affected infrared thermometers failed to comply with established quality standards. While specific inspection dates are not provided, the recall indicates a proactive response to non-compliance discovered during regulatory oversight. The company's decision to conduct a voluntary recall underscores its responsibility to address product deficiencies. Under the regulatory authority of the NMPA, companies are obligated to ensure their medical devices meet stringent safety and performance criteria. The Level III classification for this recall suggests that the non-compliance is unlikely to cause serious adverse health consequences but still warrants corrective action to protect public health. The required action for Beile (Guangzhou) Intelligent Information Technology Co., Ltd. is to retrieve all units of the specified non-compliant batch from the market, as detailed in their "Medical Device Recall Event Report Form".

Company: https://www.globalkeysolutions.net/companies/beile-guangzhou-intelligent-information-technology-co-ltd/c5fe9f11-e2b7-49fa-a8ec-7f6400a9c2c0/