# China NMPA Product Recall - Introducers & Accessories of Catheter Sheaths

Source: https://www.globalkeysolutions.net/records/china_product_recall/merit-medical-systems-inc-usa/cffc304c-8ac4-4da8-bb1c-27c4482df9cc/
Source feed: China

> China NMPA product recall for Introducers & Accessories of Catheter Sheaths by Merit Medical Systems, Inc., USA. published August 03, 2021. Recall level: Level 3 Recall. Merit Medical Systems, Inc., an American manufacturer, initiated a voluntary Class III recall of its

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Merit Medical Systems, Inc., a U.S. company, is voluntarily recalling its Introducers & Accessories for catheter sheath devices.
- Company Name: Merit Medical Systems, Inc., USA.
- Publication Date: 2021-08-03
- Product Name: Introducers & Accessories of Catheter Sheaths
- Recall Level: Level 3 Recall
- Recall Reason: The product contains an incorrect expander.
- Discovering Company: Mairuitong Medical Devices (Beijing) Co., Ltd.
- Manufacturing Company: Merit Medical Systems, Inc., USA.
- Summary: Merit Medical Systems, Inc., an American manufacturer, initiated a voluntary Class III recall of its Introducers & Accessories, which are catheter sheath devices, due to a manufacturing issue. This action was reported by Merit Medical Devices (Beijing) Co., Ltd. and publicly announced by the National Medical Products Administration (NMPA) of China on August 3, 2021. The primary concern identified was the inclusion of incorrect dilators within specific models and batches of the affected products. Dilators are crucial medical components, and an incorrect type could potentially lead to procedural complications, compromise patient safety, or render the device ineffective during use. This voluntary recall falls under the regulatory framework of the NMPA, with a Class III designation indicating that the use of or exposure to the product is unlikely to cause adverse health consequences. The required action involves the manufacturer recalling the specific problematic units. Comprehensive details regarding the affected product models, specifications, and batch numbers are documented in the accompanying "Medical Device Recall Event Report Form" referenced by the NMPA. Companies undertaking such recalls are generally expected to cease distribution, notify relevant customers, and manage the proper disposition of the recalled devices to mitigate any potential risks.

Company: https://www.globalkeysolutions.net/companies/merit-medical-systems-inc-usa/a8725617-785b-41f9-b534-625fc7e8a0a8/