# China NMPA Product Recall - Electric hydraulic operating table

Source: https://www.globalkeysolutions.net/records/china_product_recall/maikewei-shanghai-medical-equipment-co-ltd/1602e999-2048-472f-b7b6-177c955dcea1/
Source feed: China

> China NMPA product recall for Electric hydraulic operating table by Maikewei (Shanghai) Medical Equipment Co., Ltd. published April 25, 2019. Recall level: Level 2 Recall. On April 25, 2019, Maikewei (Shanghai) Medical Equipment Co., Ltd. initiated a Class II voluntary re

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Maikewei (Shanghai) Medical Equipment Co., Ltd. has initiated a voluntary recall of its electro-hydraulic operating tables.
- Company Name: Maikewei (Shanghai) Medical Equipment Co., Ltd.
- Publication Date: 2019-04-25
- Product Name: Electric hydraulic operating table
- Recall Level: Level 2 Recall
- Recall Reason: Because when the power cord plug of the electric hydraulic operating table base in some models is unplugged, the plastic socket may be pulled out of the metal frame, exposing electronic components and potentially causing personal injury, posing a safety hazard.
- Discovering Company: Maikewei (Shanghai) Medical Equipment Co., Ltd.
- Manufacturing Company: Maikewei (Shanghai) Medical Equipment Co., Ltd.
- Summary: On April 25, 2019, Maikewei (Shanghai) Medical Equipment Co., Ltd. initiated a Class II voluntary recall of specific models of its electric hydraulic operating tables. This action was taken under the regulatory oversight of the National Medical Products Administration (NMPA) and the Shanghai Food and Drug Administration, following the identification of a significant safety hazard. The primary issue involves the power cord plug of the operating table's base. When the plug is disengaged, the plastic socket may inadvertently detach from the metal frame, leading to the exposure of internal electronic components. This defect presents a potential risk of personal injury to users or patients. Maikewei (Shanghai) Medical Equipment Co., Ltd. identified this potential safety concern with products holding Registration Certificate No. 20182540273. As a proactive measure to ensure patient and user safety, the company voluntarily issued this recall. The specific models, serial numbers, and batches of the affected devices are comprehensively detailed in an accompanying Medical Device Recall Event Report Form, which serves as a crucial document for identifying and managing the impacted products. This recall underscores the company's commitment to compliance and product safety standards established by regulatory bodies like the NMPA.

Company: https://www.globalkeysolutions.net/companies/maikewei-shanghai-medical-equipment-co-ltd/77310e7c-a692-4918-a052-23f3348af2e9/