# China NMPA Product Recall - Surgilon Coated Braided Nylon No Suture and Ticron Coated Braided Polyester Nonabsorbable Suture

Source: https://www.globalkeysolutions.net/records/china_product_recall/covidien-llc/beaf1815-424a-469a-90aa-3bb43d148a1b/
Source feed: China

> China NMPA product recall for Surgilon Coated Braided Nylon No Suture and Ticron Coated Braided Polyester Nonabsorbable Suture by Covidien llc published February 06, 2024. Recall level: Level 1. Covidien LLC, a medical device manufacturer, has initiated a voluntary Class I recall of specific ba

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Covidien LLC is voluntarily recalling non-absorbable polyester sutures and non-absorbable nylon sutures.
- Company Name: Covidien llc
- Publication Date: 2024-02-06
- Product Name: Surgilon Coated Braided Nylon No Suture and Ticron Coated Braided Polyester Nonabsorbable Suture
- Recall Level: Level 1
- Recall Reason: Certain batches of non-absorbable nylon sutures and non-absorbable polyester sutures may have had sterilization doses exceeding the approved range or the approved number of ethylene oxide sterilization cycles, potentially affecting the tensile strength of the sutures in question.
- Discovering Company: Covidien Medical Devices International Trading (Shanghai) Co., Ltd.
- Manufacturing Company: Covidien llc
- Summary: Covidien LLC, a medical device manufacturer, has initiated a voluntary Class I recall of specific batches of its Surgilon Coated Braided Nylon No. Suture and Ticron Coated Braided Polyester Nonabsorbable Suture. This action, reported to the National Medical Products Administration (NMPA) on February 6, 2024, stems from a critical manufacturing deviation. The primary issue identified is that the affected sutures were subjected to sterilization processes that either exceeded the approved radiation dose range or involved more ethylene oxide sterilization cycles than permitted. This over-sterilization poses a significant concern as it may compromise the tensile strength of the sutures. Reduced tensile strength could lead to product failure during surgical procedures, potentially endangering patient safety. The recall, originating from Covidien Medical Devices International Trading (Shanghai) Co., Ltd., emphasizes the company's commitment to product integrity and patient well-being. As part of the regulatory framework overseen by the NMPA, a Class I recall signifies a situation where there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death. The required action for Covidien LLC involves the immediate removal of the affected products from the market. Further detailed information, including specific models, specifications, and batch numbers, is available in the "Medical Device Recall Event Report Form" associated with this event.

Company: https://www.globalkeysolutions.net/companies/covidien-llc/5111c5da-0a3d-4895-b59e-e49f0ad3547d/