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https://www.mhlw.go.jp/stf/houdou/0000114500.html
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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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言語切替 日本語
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言語切替 日本語
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平成28年3月02日（水）
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平成28年3月2日 照会先
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厚生労働省広報基本指針
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厚生労働省広報基本指針
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