# China NMPA Product Recall - Silicone nasal implants and facial implants

Source: https://www.globalkeysolutions.net/records/china_product_recall/hans-biomed-corp/63925003-aa9a-4132-9dd0-cab18be93fb7/
Source feed: China

> China NMPA product recall for Silicone nasal implants and facial implants by Hans Biomed Corp. published November 09, 2020. Recall level: Level 3 Recall. On November 9, 2020, the National Medical Products Administration (NMPA) and the Shanghai Municipal 

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Shanghai Hongman Trading Co., Ltd. is voluntarily recalling silicone nasal implants and facial implants.
- Company Name: Hans Biomed Corp.
- Publication Date: 2020-11-09
- Product Name: Silicone nasal implants and facial implants
- Recall Level: Level 3 Recall
- Recall Reason: The product packaging label and the instruction manual contain missing or incorrect information.
- Discovering Company: Shanghai Hongman Trading Co., Ltd.
- Manufacturing Company: Hans Biomed Corp.
- Summary: On November 9, 2020, the National Medical Products Administration (NMPA) and the Shanghai Municipal Drug Administration announced a voluntary Class III recall concerning silicone nasal and facial implants. The recall was initiated by Hans Biomed Corp., the product manufacturer, and facilitated by its agent, Shanghai Hongman Trading Co., Ltd. The primary issue prompting this action involved significant omissions or inaccuracies found on the product's outer packaging labels and within the instruction manuals. These labeling discrepancies pertained to products registered under NMPA registration number 国械注进20193131979. Importantly, the recall specifically targets certain models, specifications, and batches, as detailed in an accompanying Medical Device Recall Event Report Form, and does not impact products already in use by patients. This proactive measure underscores the commitment to regulatory compliance and patient safety, ensuring that medical devices distributed meet stringent information disclosure requirements. The voluntary recall demonstrates adherence to established medical device regulations overseen by the NMPA, aiming to rectify informational deficiencies and maintain consumer trust in product specifications.

Company: https://www.globalkeysolutions.net/companies/hans-biomed-corp/ff00a4a1-9946-473f-b288-e888404e97c6/