3 Deaths Linked To Latest Teleflex Catheter Recall

 
• By Brian Bossetta

Teleflex is recalling thousands of intra-aortic balloon catheter kits that are used during cardiac procedures and to treat complications from heart failure. This is the latest in a series of recalls from Teleflex and its subsidiary Arrow International.

Teleflex
• Source: Shutterstock

The US FDA has designated a recall from Teleflex subsidiary Arrow International class I, its most serious level.

The company recalled 16, 959 intra-aortic balloon (IAB) catheter kits distributed in the US from May 2022 through April 2024.

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