# China NMPA Product Recall - Behind-the-ear hearing aids

Source: https://www.globalkeysolutions.net/records/china_product_recall/hunan-kefu-medical-technology-development-co-ltd/a56cd015-97fc-49ec-9806-ed6513dc6e27
Source feed: China

> China NMPA product recall for Behind-the-ear hearing aids by Hunan Kefu Medical Technology Development Co., Ltd. published December 09, 2019. Recall level: Level 3. The National Medical Products Administration (NMPA) published an announcement on December 9, 2019, d

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Hunan Kefu Medical Technology Development Co., Ltd. voluntarily recalls behind-the-ear hearing aids
- Company Name: Hunan Kefu Medical Technology Development Co., Ltd.
- Publication Date: 2019-12-09
- Product Name: Behind-the-ear hearing aids
- Recall Level: Level 3
- Recall Reason: The product was found to have indicators that did not meet the product's technical requirements after being subject to provincial-level supervision and spot checks by the Hangzhou Municipal Market Supervision and Administration Bureau.
- Discovering Company: Hunan Kefu Medical Technology Development Co., Ltd.
- Manufacturing Company: Hunan Kefu Medical Technology Development Co., Ltd.
- Summary: The National Medical Products Administration (NMPA) published an announcement on December 9, 2019, detailing a Class III voluntary recall initiated by Hunan Kefu Medical Technology Development Co., Ltd. for its behind-the-ear hearing aids. The recall was prompted by the discovery that the company's manufactured hearing aids, under registration number "xiang xie zhu zhun 20182190162," specifically model KFZTQMB011 and batch P20190114 (10 units), did not comply with their registered product technical requirements. This non-conformance was identified through a provincial-level supervision and spot check performed by the Hangzhou Municipal Market Supervision Administration, which found that product indicators failed to meet established specifications.

Under the NMPA's regulatory guidance, Hunan Kefu Medical Technology Development Co., Ltd. is mandated to undertake several corrective actions. These include immediately notifying all distributors in China to halt sales of the affected batch and return the products to the factory for rework. Additionally, the company is required to conduct a comprehensive internal self-inspection to identify the root causes of the non-compliance and develop specific improvement measures to prevent similar issues in the future. These actions are crucial for maintaining adherence to medical device regulations and ensuring product quality.

Company: https://www.globalkeysolutions.net/companies/hunan-kefu-medical-technology-development-co-ltd/5552cac0-1a47-42db-9b3a-9cba24693551