# China NMPA Product Recall - Spine Instruments surgical instrument kit

Source: https://www.globalkeysolutions.net/records/china_product_recall/stryker-spine-inc/80068865-3131-402f-b81d-9a3498fcee41/
Source feed: China

> China NMPA product recall for Spine Instruments surgical instrument kit by Stryker Spine Inc. published December 20, 2023. Recall level: Level 3 Recall. On December 20, 2023, the National Medical Products Administration (NMPA) announced a Class III volu

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Stryker Spine Corporation is voluntarily recalling spinal surgery instrument kits.
- Company Name: Stryker Spine Inc.
- Publication Date: 2023-12-20
- Product Name: Spine Instruments surgical instrument kit
- Recall Level: Level 3 Recall
- Recall Reason: A specific model and batch of bone retractors used incorrect clamping components, causing the bone retractors to fail to attach to the arm column axis of the hospital bed.
- Discovering Company: Stryker (Beijing) Medical Devices Co., Ltd.
- Manufacturing Company: Stryker Spine Inc.
- Summary: On December 20, 2023, the National Medical Products Administration (NMPA) announced a Class III voluntary recall initiated by Stryker Spine Corporation concerning its Spine Surgical Instrument Kits, specifically those registered under National Medical Device Registration No. 20160323. This crucial action follows the discovery of a significant manufacturing defect within a particular model and batch of bone retractors. The core issue involves the incorporation of incorrect clamping components. As a direct consequence, these affected bone retractors are rendered incapable of securely connecting to the arm column axis of the surgical bed, which is a critical functionality for spinal surgical procedures. The recall was reported by Stryker (Beijing) Medical Devices Co., Ltd., highlighting the company’s responsibility in identifying and addressing product deficiencies. The Class III designation indicates that while the issue is not immediately life-threatening, it could lead to temporary health problems or pose a slight threat of serious harm if not corrected. This voluntary recall demonstrates Stryker's adherence to regulatory standards set by the NMPA and their commitment to product quality and patient safety. Specific details regarding the affected product models, specifications, and batch information are available in the comprehensive "Medical Device Recall Event Report Form" provided by the company, ensuring transparency and facilitating the effective removal of these instruments from circulation.

Company: https://www.globalkeysolutions.net/companies/stryker-spine-inc/956029de-236c-4bfa-9fed-349cddcd8864/