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Home » Three Recalls: A Heart Pump Associated With 49 Deaths, a Resuscitator, and an Infusion System
Three Recalls: A Heart Pump Associated With 49 Deaths, a Resuscitator, and an Infusion System
The FDA has identified product recalls for Vyaire’s AirLife Manual Resuscitators and for the use instructions for Abiomed’s left-sided heart pumps as Class I, while device manufacturer InfuTronix is voluntarily recalling its line of Nimbus Infusion Pumps after design flaws prompted thousands of customer complaints.