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医療機器自主回収のお知らせ（クラスI：バルーンポンピング用カテーテル）｜厚生労働省

https://www.mhlw.go.jp/stf/houdou/0000114500.html

April 7, 2026 at 03:00 AM JST•The archive page, viewer, and downloads use this saved version.

April 7, 2026 at 03:00 AM JST·www.mhlw.go.jp

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医療機器自主回収のお知らせ（クラスI：バルーンポンピング用カテーテル）｜厚生労働省

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Original URLhttps://www.mhlw.go.jp/stf/houdou/0000114500.html

StartedApril 7, 2026 at 03:00 AM JST

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This page announces a Class I medical device voluntary recall by Teleflex Medical Japan Co., Ltd. The company is recalling the "Arrow RedyGuard IABP Catheter Set" (intra-aortic balloon pumping catheter). The recall covers two product numbers (IAB-06830U and IAB-06840U) with multiple specified lot numbers. The recall notice was provided by Tokyo authorities on March 2, 2016, and is classified as a serious safety issue requiring immediate action from healthcare facilities using these devices.

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