# China NMPA Product Recall - Comprehens System

Source: https://www.globalkeysolutions.net/records/china_product_recall/biomet-orthopedics/2af29111-3933-4e39-8ba0-911f88a6a448/
Source feed: China

> China NMPA product recall for Comprehens System by Biomet Orthopedics published March 28, 2025. Recall level: Level 3 Recall. Biomet Orthopedics has voluntarily initiated a Class III recall for its Comprehends System Shoulder 

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Biomet Orthopedics initiates voluntary recall of shoulder joint systems.
- Company Name: Biomet Orthopedics
- Publication Date: 2025-03-28
- Product Name: Comprehens System
- Recall Level: Level 3 Recall
- Recall Reason: The product inserter is difficult to install or remove.
- Discovering Company: Zimmer Medical (Shanghai) International Trading Co., Ltd.
- Manufacturing Company: Biomet Orthopedics
- Summary: Biomet Orthopedics has voluntarily initiated a Class III recall for its Comprehends System Shoulder Joint System, as formally reported to the National Medical Products Administration (NMPA) by Zimmer Medical (Shanghai) International Trading Co., Ltd. The core issue precipitating this recall stems from observed difficulties during the installation or removal of the product inserter. This performance flaw raises concerns about the potential for complications during surgical procedures, which could inadvertently compromise patient safety and procedural efficiency. The NMPA, China's primary regulatory authority for medical products, is overseeing this action, which has been designated as a Class III recall, indicating that the product issue is unlikely to cause serious adverse health consequences but warrants corrective action. The provided documentation does not specify any inspection dates related to the initiation of this recall. As part of the required actions, Biomet Orthopedics is actively recalling the affected Comprehends System units. Comprehensive details regarding the specific models, product specifications, and batch numbers implicated in this recall are formally documented within an accompanying 'Medical Device Recall Event Report Form.' This voluntary recall underscores the manufacturer's commitment to addressing product performance issues proactively to maintain device safety and ensure compliance with regulatory standards.

Company: https://www.globalkeysolutions.net/companies/biomet-orthopedics/9bcf230e-90e5-4f4e-8673-6456e0ed8783/