# China NMPA Product Recall - NexGen pre-coated tibial disc trunk components

Source: https://www.globalkeysolutions.net/records/china_product_recall/zimmer-inc/4b799a0e-6074-4632-8894-5ea928e0ce14/
Source feed: China

> China NMPA product recall for NexGen pre-coated tibial disc trunk components by Zimmer Inc. published April 14, 2015. Recall level: Class II Recall. Zimmer (Shanghai) Medical International Trading Co., Ltd. initiated a voluntary Class II recall on A

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Zimmer Medical (Shanghai) International Trading Co., Ltd. voluntarily recalls knee prostheses.
- Company Name: Zimmer Inc.
- Publication Date: 2015-04-14
- Product Name: NexGen pre-coated tibial disc trunk components
- Recall Level: Class II Recall
- Recall Reason: A specific batch of NexGen pre-coated tibial disc dry components may have an internal taper dimension that exceeds the expected size, which could cause the components used with it to not be fully locked.
- Discovering Company: Zimmer Medical (Shanghai) International Trading Co., Ltd.
- Manufacturing Company: Zimmer Inc.
- Summary: Zimmer (Shanghai) Medical International Trading Co., Ltd. initiated a voluntary Class II recall on April 14, 2015, concerning a specific batch of NexGen pre-coated tibial disc trunk components. The company, in collaboration with its manufacturer Zimmer Inc. and Zimmer GmbH, identified a manufacturing defect where the internal taper dimension of lot number 62283417 (product number 00-5980-037-02) exceeded its intended size. This critical deviation posed a significant risk: the affected components might not fully lock when used in cemented knee joint prostheses, potentially compromising the stability and functionality of knee replacements. The recall specifically targeted 32 units of these components that were imported, produced, and sold within China. This action was undertaken in accordance with the regulatory guidelines of the National Medical Products Administration (NMPA), emphasizing the company's commitment to patient safety and product quality standards. As a direct corrective measure, all identified defective products were promptly retrieved and returned to the manufacturer, Zimmer Inc. This ensures that the non-conforming components are removed from circulation, mitigating potential patient harm and upholding regulatory compliance.

Company: https://www.globalkeysolutions.net/companies/zimmer-inc/05cec43c-1d05-4504-b41e-c83d04872937/