# China NMPA Product Recall - Knee prosthesis - tibial pad

Source: https://www.globalkeysolutions.net/records/china_product_recall/zimmer-trabecular-metal-technology-inc/d2c81105-0966-4acd-aa11-dee5dcd10b2e/
Source feed: China

> China NMPA product recall for Knee prosthesis - tibial pad by Zimmer Trabecular Metal Technology, Inc. published February 19, 2019. Recall level: Level 2 Recall. Zimmer Trabecular Metal Technology, Inc. voluntarily initiated a Class II recall for specific knee p

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Zimmer Trabecular Metal Technology, Inc. is issuing a proactive recall of its knee prosthesis – the tibial pad.
- Company Name: Zimmer Trabecular Metal Technology, Inc.
- Publication Date: 2019-02-19
- Product Name: Knee prosthesis - tibial pad
- Recall Level: Level 2 Recall
- Recall Reason: The product inside the box may not match the product indicated on the label.
- Discovering Company: Zimmer Medical (Shanghai) International Trading Co., Ltd.
- Manufacturing Company: Zimmer Trabecular Metal Technology, Inc.
- Summary: Zimmer Trabecular Metal Technology, Inc. voluntarily initiated a Class II recall for specific knee prostheses, specifically tibial pads, which was reported to China's National Medical Products Administration (NMPA) by its agent, Zimmer (Shanghai) Medical International Trading Co., Ltd., on February 19, 2019. The fundamental concern prompting this action was the potential for a mismatch between the actual product inside the packaging and the information printed on its label.The recall encompasses seven distinct batches of 5mm Tibial Pads, including both Right Outer/Left Inner and Left Outer/Right Inner configurations, all sized 4. These critical components are integral to the Trabecular Metal knee joint system, designed for total knee arthroplasty in patients suffering from severe knee degeneration, trauma, or other pathological conditions requiring fixation with bone cement.Under the NMPA's regulatory framework for medical devices, a Class II recall signifies a situation where the use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. Although the recall report was filed in China, the document explicitly confirms that none of the affected batches were sold or imported into the Chinese market. The primary regions impacted by this recall include the USA, Canada, Japan, and the European Union. The required action involves the systematic removal of these identified batches from distribution to mitigate risks associated with incorrect labeling, thereby upholding product integrity and patient safety.

Company: https://www.globalkeysolutions.net/companies/zimmer-trabecular-metal-technology-inc/5829618a-daa8-4c3b-bc35-5f4453ba8be5/