# China NMPA Product Recall - Hip joint scaffold

Source: https://www.globalkeysolutions.net/records/china_product_recall/howmedicaosteonics-corp/e0620234-782a-4c7f-9dd4-3e830e82cf8f/
Source feed: China

> China NMPA product recall for Hip joint scaffold by HowmedicaOsteonics Corp. published October 29, 2019. Recall level: Level 3 Recall. Howmedica Osteonics Corp., a medical device manufacturer, initiated a voluntary Class III recall of 

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Howmedica Osteonics Corp. voluntarily recalls hip joint meshwork.
- Company Name: HowmedicaOsteonics Corp.
- Publication Date: 2019-10-29
- Product Name: Hip joint scaffold
- Recall Level: Level 3 Recall
- Recall Reason: The issue involves the mixed packaging of small and medium-sized round wire mesh frames.
- Discovering Company: Stryker (Beijing) Medical Devices Co., Ltd.
- Manufacturing Company: HowmedicaOsteonics Corp.
- Summary: Howmedica Osteonics Corp., a medical device manufacturer, initiated a voluntary Class III recall of its hip joint mesh frames (NMPA Registration No.: 20173466294). This recall, reported by Stryker (Beijing) Medical Devices Co., Ltd. and publicized by the National Medical Products Administration (NMPA) on October 29, 2019, addresses a significant packaging issue. The core problem identified is the mixed packaging of small and medium-sized round mesh frames, meaning incorrect sizes could be present in the product packaging.

This packaging anomaly creates a potential risk for healthcare professionals, as using an incorrectly sized hip joint mesh frame during surgery could lead to compromised patient safety and less than optimal surgical results. A Class III recall indicates that the use of or exposure to the affected product is unlikely to cause adverse health consequences, yet the issue warrants corrective action.

Under the NMPA's regulatory guidance, Howmedica Osteonics Corp. is required to take specific actions to mitigate this risk. These actions involve the comprehensive identification, segregation, and removal of all affected product batches from the market. Detailed information regarding the specific models, specifications, and batch numbers of the recalled products is available in the associated "Medical Device Recall Event Report Form." This prompt action emphasizes the company's commitment to maintaining product quality and ensuring patient safety within the NMPA's robust regulatory environment.

Company: https://www.globalkeysolutions.net/companies/howmedicaosteonics-corp/fb8e59ba-c29a-43ec-b211-2e0a543aa1f7/