# China NMPA Product Recall - Achilles tendon suture guide

Source: https://www.globalkeysolutions.net/records/china_product_recall/newdeal-sas/42273bd1-b2ce-47ff-a5bc-b2c1013e0107
Source feed: China

> China NMPA product recall for Achilles tendon suture guide by NEWDEAL SAS published December 07, 2016. Recall level: Level 3 Recall. The National Medical Products Administration (NMPA) announced a Level III voluntary recall initiated

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: General Medical Devices (Shanghai) Co., Ltd. is voluntarily recalling its Achilles tendon suture guide.
- Company Name: NEWDEAL SAS
- Publication Date: 2016-12-07
- Product Name: Achilles tendon suture guide
- Recall Level: Level 3 Recall
- Recall Reason: Some models/lots of Tyvek Achilles tendon suture guides may not maintain the integrity of their seal within the claimed sterilization period of the outer packaging, potentially affecting the sterility of the outer surface of the inner packaging.
- Discovering Company: General Medical Equipment (Shanghai) Co., Ltd.
- Manufacturing Company: NEWDEAL SAS
- Summary: The National Medical Products Administration (NMPA) announced a Level III voluntary recall initiated by General Medical Devices (Shanghai) Co., Ltd., on behalf of manufacturer NPUPAL SAS (also referred to as Newdeal SAS). The recall, reported on December 7, 2016, concerns the Achilles Tendon Suture Guide (Model 119700, various batch numbers like F4FV/FAFV). The primary issue identified was a potential defect in the Tyvek seal of the product’s outer sterile packaging. It was discovered that a portion of these seals might not maintain integrity throughout the claimed sterilization period, posing a risk to the sterility of the *outer surface* of the inner packaging. However, internal verification confirmed that the medical device itself, contained within the inner packaging, retained its sterility, and no complaints or adverse events related to this issue had been reported. Operating under NMPA's regulatory framework for medical device recalls, the manufacturer implemented several required actions. These included conducting a comprehensive safety assessment to evaluate the risk, thoroughly checking inventory with all relevant distributors globally, and requesting the immediate return of all affected products. This proactive measure aims to ensure product quality and patient safety, despite the confirmed sterility of the device itself and the low-risk classification of the recall.

Company: https://www.globalkeysolutions.net/companies/newdeal-sas/6be0139b-8aa1-42b4-a44a-d1d60a2aa86f