# China NMPA Product Recall - Thoracic and laparoscopic endoscopy

Source: https://www.globalkeysolutions.net/records/china_product_recall/olympus-vieinte-and-yibei-company/37a1d94c-d8e2-4787-8ccd-76818bae9b40/
Source feed: China

> China NMPA product recall for Thoracic and laparoscopic endoscopy by Olympus Vieinte and Yibei Company published November 13, 2024. Recall level: Level 3 Recall. On November 13, 2024, Olympus Trading (Shanghai) Co., Ltd. officially reported a voluntary Class III

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Olympus Viente and E-BetX are voluntarily recalling thoracic and laparoscopic endoscopes.
- Company Name: Olympus Vieinte and Yibei Company
- Publication Date: 2024-11-13
- Product Name: Thoracic and laparoscopic endoscopy
- Recall Level: Level 3 Recall
- Recall Reason: The product was mistakenly sent to the customer and used.
- Discovering Company: Olympus Trading (Shanghai) Co., Ltd.
- Manufacturing Company: Olympus Vieinte and Yibei Company
- Summary: On November 13, 2024, Olympus Trading (Shanghai) Co., Ltd. officially reported a voluntary Class III recall concerning thoracic and laparoscopic endoscopes manufactured by Olympus Viente and E-Tech. This significant action was prompted by a critical issue involving the incorrect shipment and subsequent use of these medical devices by customers, leading to a potential deviation from intended use or safety protocols. The recalled products are identifiable by National Medical Device Registration Certificate No. 20212060441. A key aspect of this recall is the clarification that none of the specific products involved in this event were imported into China, suggesting the issue primarily impacted other markets or was contained before reaching the Chinese distribution channels. This voluntary recall, undertaken by the manufacturers and reported by Olympus Trading (Shanghai) Co., Ltd., demonstrates adherence to the regulatory expectations set forth by the National Medical Products Administration (NMPA). The company has provided comprehensive details regarding the specific models, specifications, and batches affected in an attached "Medical Device Recall Event Report Form." This proactive measure underscores a commitment to product safety and quality assurance, addressing potential risks arising from distribution errors before they could impact the local market.

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