# China NMPA Product Recall - High-frequency ablation electrode, pediatric urological optical endoscope and accessories

Source: https://www.globalkeysolutions.net/records/china_product_recall/olympus-vieinte-and-yibei-company/59ebefef-518e-414f-9d02-644a62b5852a/
Source feed: China

> China NMPA product recall for High-frequency ablation electrode, pediatric urological optical endoscope and accessories by Olympus Vieinte and Yibei Company published August 29, 2023. Recall level: Level 2 Recall. Olympus Trading (Shanghai) Co., Ltd. has initiated a voluntary Class II recall, reported to the Nati

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Olympus Winter & Ibe GmbH is voluntarily recalling high-frequency ablation electrodes, pediatric urological optical endoscopes, and accessories.
- Company Name: Olympus Vieinte and Yibei Company
- Publication Date: 2023-08-29
- Product Name: High-frequency ablation electrode, pediatric urological optical endoscope and accessories
- Recall Level: Level 2 Recall
- Recall Reason: The Japanese instruction manual contains an error.
- Discovering Company: Olympus Trading (Shanghai) Co., Ltd.
- Manufacturing Company: Olympus Vieinte and Yibei Company
- Summary: Olympus Trading (Shanghai) Co., Ltd. has initiated a voluntary Class II recall, reported to the National Medical Products Administration (NMPA), concerning medical devices manufactured by Olympus Winter & Ibe GmbH. The recall, announced on August 29, 2023, addresses critical errors identified within the Japanese instruction manuals accompanying the affected products.The recalled devices include high-frequency resection electrodes, pediatric urological optical endoscopes and their accessories, and high-frequency ablation electrodes. While no specific inspection dates were provided in the document, this action aligns with the regulatory framework requiring manufacturers to ensure the clarity and correctness of all product information. The primary issue stems from these documentation inaccuracies, which could potentially impact user understanding or device operation.The required action involves the voluntary removal of these products from the market to rectify the identified manual errors. The Class II designation implies that the use of or exposure to the violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote. Further details regarding specific affected models are available in the 'Medical Device Recall Event Report Form' submitted to the NMPA.

Company: https://www.globalkeysolutions.net/companies/olympus-vieinte-and-yibei-company/614a3096-52f4-4eaa-9d5d-41ef0a7e55f7/