Domestic Class I Recall: Two Renowned Medical Device Companies Recall 267,000 Devices

Mar 27, 2024 18:13 CST Updated 18:13

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Source: National Medical Products Administration

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The National Medical Products Administration (NMPA) has recently released Level 1 recall information for Medtronic and Arrow in China. The product defects are as follows for your reference:

Medtronic Issues Level 1 Recall of 12,367 External Drainage Devices in China

Medtronic (Shanghai) Management Co., Ltd. reported,Due to the risk of disconnection in the tubing of the external drainage device, etc.Medtronic Inc., the manufacturer, voluntarily recalled its External Drainage and Monitoring System (China Medical Device Registration No. 20183140246). The recall level is Class I.

Arrow International Inc. Issues Level 1 Recall in China for 254,850 Arterial Puncture Catheter Kits

Teleflex Medical Trading (Shanghai) Co., Ltd. reported,Due to possible resistance during the use of the guidewire handle/lumen, etc.Arrow International LLC Initiates Recall of Arterial Puncture Catheter Kits (Registration No.: China Medical Device Registration No. 20163032161). The recall is classified as Level I.

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