# China NMPA Product Recall - Self-adhesive dressing

Source: https://www.globalkeysolutions.net/records/china_product_recall/minnesota-mining-manufacturing-medical-devices-shanghai-co-ltd/e0f640b7-349e-4a76-90a0-23a0dc443fdb/
Source feed: China

> China NMPA product recall for Self-adhesive dressing by Minnesota Mining Manufacturing Medical Devices (Shanghai) Co., Ltd. published February 21, 2017. Recall level: Level III. On February 21, 2017, Minnesota Mining Manufacturing Medical Devices (Shanghai) Co., Ltd., a subsidi

---

## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Minnesota Mining Manufacturing Medical Devices (Shanghai) Co., Ltd. is voluntarily recalling its self-adhesive dressings.
- Company Name: Minnesota Mining Manufacturing Medical Devices (Shanghai) Co., Ltd.
- Publication Date: 2017-02-21
- Product Name: Self-adhesive dressing
- Recall Level: Level III
- Recall Reason: Some product labels lack production dates; this is to comply with Chinese regulations.
- Discovering Company: Minnesota Mining Manufacturing Medical Devices (Shanghai) Co., Ltd.
- Manufacturing Company: Minnesota Mining Manufacturing Medical Devices (Shanghai) Co., Ltd.
- Summary: On February 21, 2017, Minnesota Mining Manufacturing Medical Devices (Shanghai) Co., Ltd., a subsidiary of 3M Company, initiated a voluntary Class III recall of certain self-adhesive dressings. This action was taken to ensure compliance with Chinese regulatory requirements overseen by the National Medical Products Administration (NMPA). The primary issue identified was the absence of production dates on some product labels, a critical component for product traceability and consumer safety in medical devices. While no specific inspection dates were provided in the recall document, the company's self-reporting and subsequent recall demonstrate its commitment to addressing product non-conformities within the established regulatory framework. The required action involved a voluntary Class III recall, indicating that the use of or exposure to the violative product is not likely to cause adverse health consequences. Details regarding specific product numbers, specifications, and batch numbers were referenced in an accompanying 'Medical Device Recall Event Report Form', outlining a structured approach to managing the recall. This ensures that all distributed products meet the stipulated labeling criteria, thereby protecting public health and maintaining regulatory compliance.

Company: https://www.globalkeysolutions.net/companies/minnesota-mining-manufacturing-medical-devices-shanghai-co-ltd/ae45d687-fda6-45c4-a54b-3fd4bcbfd852/