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Medtronic Endotracheal Tubes Subject Of Class I Recall

 
• By Brian Bossetta

The US FDA has designated an April recall of tens of thousands of Medtronic devices as class I due to the potential of airway obstruction during surgery.

Sign of Medtronic at Canada Headquarters in Brampton, Ontario, Canada.
• Source: Shutterstock

The US Food and Drug Administration has hit device giant Medtronic with another class I recall, this time for electromyogram (EMG) endotracheal tubes used during surgery while the patient is under anesthesia.

The April recall included 625,748 NIM Standard Reinforced EMG and NIM CONTACT Reinforced EMD endotracheal tubes distributed globally.

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