FDA alerts to Class I recall of Nimbus, Nimbus II Infusion Pump Systems due to multiple potential failure modes
According to the FDA, InfuTronix LLC has recalled the Nimbus Administration Set, Flex, and PainPro (also known as the Halo Ambulatory Infusion System), in addition to the Nimbus II PainPRO, Flex, Plus, EpiD, and EMS infusion pumps, due to several potential modes of product failure.