# China NMPA Product Recall - Band-Aid

Source: https://www.globalkeysolutions.net/records/china_product_recall/jinhua-jingdi-medical-supplies-co-ltd/709eeeb5-460b-43ac-9de9-67fe11842ce4/
Source feed: China

> China NMPA product recall for Band-Aid by Jinhua Jingdi Medical Supplies Co., Ltd. published September 11, 2017. Recall level: Level 3 Recall. Jinhua Jingdi Medical Supplies Co., Ltd. initiated a voluntary Class III recall of its band-aids (re

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Jinhua Jingdi Medical Supplies Co., Ltd. voluntarily recalls its bandages.
- Company Name: Jinhua Jingdi Medical Supplies Co., Ltd.
- Publication Date: 2017-09-11
- Product Name: Band-Aid
- Recall Level: Level 3 Recall
- Recall Reason: The instruction manual attached to the product packaging bag was missing three parts during the printing process: the production address, service hotline, and product technical requirements number. This is a packaging defect.
- Discovering Company: Jinhua Jingdi Medical Supplies Co., Ltd.
- Manufacturing Company: Jinhua Jingdi Medical Supplies Co., Ltd.
- Summary: Jinhua Jingdi Medical Supplies Co., Ltd. initiated a voluntary Class III recall of its band-aids (registration number Zhejinxiebei 20150022), a measure publicly reported by the National Medical Products Administration (NMPA) on September 11, 2017. This action stemmed from a identified packaging defect where the instruction manuals, accompanying specific batches (20160901 and 20170101), were found to be missing critical regulatory information. The omissions included the product's official production address, a customer service hotline, and the designated product technical requirements number. Despite these informational discrepancies, the company confirmed that the band-aids themselves met all specified performance and technical quality standards. The recall, impacting 80 units of "Sunflower brand high-elasticity comfort bandage" sold within China, was undertaken as a proactive measure. The company's objective was to mitigate subsequent regulatory risks associated with incomplete labeling, demonstrating adherence to the stringent guidelines set forth by the NMPA for medical devices. Jinhua Jingdi Medical Supplies Co., Ltd. formally documented the recall through a "Medical Device Recall Event Report Form" submitted to the relevant Provincial Food and Drug Administration, detailing the affected models and batch numbers. This highlights the regulatory framework requiring manufacturers to ensure comprehensive and accurate product information is provided to consumers.

Company: https://www.globalkeysolutions.net/companies/jinhua-jingdi-medical-supplies-co-ltd/e2896dac-d759-472b-a194-b2e450120562/