# China NMPA Product Recall - Jiangxi Guokang Industrial Co., Ltd., Jiangxi Baishikang Medical Device Co., Ltd., Jiangxi Fenglin Medical Technology Co., Ltd., Nanchang Houpu Medical Device Co., Ltd.

Source: https://www.globalkeysolutions.net/records/china_product_recall/jiangxi-guokang-industrial-co-ltd-jiangxi-baishikang-medical-device-co-ltd-jiangxi-fenglin-medical-technology-co-ltd-nanchang-houpu-medical-device-co-ltd/1852b955-7b47-4c42-884c-98f76478b181/
Source feed: China

> China NMPA product recall for  by Jiangxi Guokang Industrial Co., Ltd., Jiangxi Baishikang Medical Device Co., Ltd., Jiangxi Fenglin Medical Technology Co., Ltd., Nanchang Houpu Medical Device Co., Ltd. published October 29, 2020. Recall level: . The National Medical Products Administration (NMPA) released a significant announcement on October 2

---

## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Medical Device Voluntary Recall Notice (October 28, 2020)
- Company Name: Jiangxi Guokang Industrial Co., Ltd., Jiangxi Baishikang Medical Device Co., Ltd., Jiangxi Fenglin Medical Technology Co., Ltd., Nanchang Houpu Medical Device Co., Ltd.
- Publication Date: 2020-10-29
- Recall Reason: Product defective
- Discovering Company: Jiangxi Guokang Industrial Co., Ltd., Jiangxi Baishikang Medical Device Co., Ltd., Jiangxi Fenglin Medical Technology Co., Ltd., Nanchang Houpu Medical Device Co., Ltd.
- Manufacturing Company: Jiangxi Guokang Industrial Co., Ltd., Jiangxi Baishikang Medical Device Co., Ltd., Jiangxi Fenglin Medical Technology Co., Ltd., Nanchang Houpu Medical Device Co., Ltd.
- Summary: The National Medical Products Administration (NMPA) released a significant announcement on October 29, 2020, detailing a voluntary recall of medical devices initiated on October 28, 2020. This action involved four distinct companies: Jiangxi Guokang Industrial Co., Ltd., Jiangxi Baishikang Medical Device Co., Ltd., Jiangxi Fenglin Medical Technology Co., Ltd., and Nanchang Houpu Medical Device Co., Ltd. Each company proactively undertook the recall of their respective products due to identified issues categorizing them as 'substandard medical devices.' This regulatory intervention by the NMPA underscores its commitment to ensuring the quality and safety of medical products available to the public within its jurisdiction. The voluntary nature of the recall indicates the companies' compliance with regulatory expectations and their responsibility in addressing product deficiencies. While specific details regarding the nature of the 'substandard' designation are referenced in accompanying recall event report forms, the overarching regulatory framework mandates that manufacturers address product quality concerns to protect patient health. The required action for these companies was to execute a comprehensive recall, removing the non-compliant devices from circulation to prevent potential harm.

Company: https://www.globalkeysolutions.net/companies/jiangxi-guokang-industrial-co-ltd-jiangxi-baishikang-medical-device-co-ltd-jiangxi-fenglin-medical-technology-co-ltd-nanchang-houpu-medical-device-co-ltd/bd4bc7b9-2649-483d-9409-a87ab07a255a/