# China NMPA Product Recall - Spinal internal fixation system

Source: https://www.globalkeysolutions.net/records/china_product_recall/medtronic-sofamor-danek-usa-inc/0a86d935-52f6-4324-a018-c270c271d218/
Source feed: China

> China NMPA product recall for Spinal internal fixation system by Medtronic Sofamor Danek USA, Inc. published April 03, 2020. Recall level: Level 2 Recall. Medtronic Sofamor Danek USA, Inc., in cooperation with its affiliate Medtronic (Shanghai) Management

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Medtronic Sofamor Danek USA, Inc. is issuing a voluntary recall of its spinal fixation system.
- Company Name: Medtronic Sofamor Danek USA, Inc.
- Publication Date: 2020-04-03
- Product Name: Spinal internal fixation system
- Recall Level: Level 2 Recall
- Recall Reason: The issue involves a discrepancy between the actual total length and the markings on a certain batch number of type 6958838 universal screws.
- Discovering Company: Medtronic (Shanghai) Management Co., Ltd.
- Manufacturing Company: Medtronic Sofamor Danek USA, Inc.
- Summary: Medtronic Sofamor Danek USA, Inc., in cooperation with its affiliate Medtronic (Shanghai) Management Co., Ltd., initiated a voluntary Class II recall for its spinal internal fixation system. This recall, reported to the National Medical Products Administration (NMPA) on April 3, 2020, specifically targets the 6958838 model universal screw, registered under Certificate No.: 20173460615. The core issue prompting this action is a critical discrepancy: the actual total length of the universal screw does not match the length indicated in its markings. Such an inconsistency could potentially affect surgical outcomes and patient safety by leading to incorrect device selection or implantation during spinal procedures. The Class II designation by the NMPA indicates that the use of, or exposure to, the affected product may cause temporary or medically reversible adverse health consequences, or that the probability of serious adverse health consequences is remote.

Under the regulatory framework of the NMPA, Medtronic is required to conduct a thorough recall to remove all affected products from circulation. While the document does not specify inspection dates, the voluntary recall itself acts as the primary regulatory action in response to the identified product non-conformity. Detailed information regarding the specific affected product models, specifications, and batch numbers is available in the accompanying "Medical Device Recall Event Report Form." This ensures a comprehensive retrieval process, aimed at mitigating potential risks and upholding the quality and safety standards for medical devices within China as overseen by the NMPA.

Company: https://www.globalkeysolutions.net/companies/medtronic-sofamor-danek-usa-inc/3dae4c6c-7556-4da9-a13d-28702559ac2b/