# China NMPA Product Recall - Infrared thermometer

Source: https://www.globalkeysolutions.net/records/china_product_recall/beile-guangzhou-intelligent-information-technology-co-ltd/8820ee20-32a0-4d1c-88c1-0ee36f0e17e4
Source feed: China

> China NMPA product recall for Infrared thermometer by Beile (Guangzhou) Intelligent Information Technology Co., Ltd. published January 10, 2022. Recall level: Level 2 Recall. Beile (Guangzhou) Intelligent Information Technology Co., Ltd. has initiated a voluntary recall of i

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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: 2022-01-10
- Product Name: Infrared thermometer
- Recall Level: Level 2 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 recall of its infrared thermometers, following the discovery of non-compliance during routine random inspections. The affected products bear production batch numbers 200924A02 and 2001151500D5, under Registration Certificate No. 粤械注准20202070777. This significant regulatory action, announced on January 10, 2022, is under the purview of the National Medical Products Administration (NMPA), the primary regulatory body responsible for medical devices in China. The company's decision to proactively recall these devices highlights a commitment to addressing product quality issues that could potentially impact user safety and accuracy. The specific nature of the non-compliance was identified through standard inspection processes designed to ensure medical devices meet stringent quality and performance criteria. While the exact details of the deviation from standards are provided in the 'Medical Device Recall Event Report Form,' the overarching requirement is for the company to remove these non-compliant infrared thermometers from the market. This voluntary recall mechanism allows manufacturers to take prompt corrective action when product deficiencies are identified, thereby mitigating potential risks to public health and maintaining consumer trust in medical devices.

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