# China NMPA Product Recall - Otolaryngology surgical navigation system, spinal surgery surgical navigation system, neurosurgery surgical navigation system

Source: https://www.globalkeysolutions.net/records/china_product_recall/medtronic-navigation-inc/12cd2170-f318-4596-b574-c751e1f12067/
Source feed: China

> China NMPA product recall for Otolaryngology surgical navigation system, spinal surgery surgical navigation system, neurosurgery surgical navigation system by Medtronic Navigation Inc. published December 05, 2023. Recall level: Level 2 Recall. Medtronic Navigation, Inc. has initiated a voluntary Level II recall of its Otolaryngology Surgical 

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Medtronic Navigation, Inc. is voluntarily recalling its ENT surgical navigation systems, spinal surgical navigation systems, and neurosurgical navigation systems.
- Company Name: Medtronic Navigation Inc.
- Publication Date: 2023-12-05
- Product Name: Otolaryngology surgical navigation system, spinal surgery surgical navigation system, neurosurgery surgical navigation system
- Recall Level: Level 2 Recall
- Recall Reason: A software bug exists in versions 2.0 and 2.0.1 of the StealthStation™ S8 software application.
- Discovering Company: Medtronic (Shanghai) Management Co., Ltd.
- Manufacturing Company: Medtronic Navigation Inc.
- Summary: Medtronic Navigation, Inc. has initiated a voluntary Level II recall of its Otolaryngology Surgical Navigation Systems, Spinal Surgery Surgical Navigation Systems, and Neurosurgery Surgical Navigation Systems. The recall, reported by Medtronic (Shanghai) Management Co., Ltd. and published by the National Medical Products Administration (NMPA) on December 5, 2023, stems from identified software anomalies. Specifically, versions 2.0 and 2.0.1 of the StealthStation™ S8 software application contain defects that necessitate this corrective action. While no specific inspection dates are detailed in the document, the NMPA oversees this regulatory action, highlighting its commitment to medical device safety. The company is required to provide a comprehensive "Medical Device Recall Event Report Form" outlining affected product models, specifications, and batches. This recall underscores the importance of stringent software quality control within the medical device industry to ensure patient safety and device efficacy.

Company: https://www.globalkeysolutions.net/companies/medtronic-navigation-inc/314c41df-1248-4c0a-88d1-30388476ffd7/