U.S. Food and Drug Admin Recall - Laryngoscope

Please note, the Food and Drug Administration has issued a Laryngoscope Recall. Medtronic has removed certain McGrath MAC video Laryngoscopes, and has issued updates to use instructions for others due to increased risk for battery overheating and explosion.

Medtronic is recalling certain devices and updating use instructions for another due to the possibility that the battery may deplete below its designed threshold. If this happens, it increases the risk of battery instability and may lead to increased battery temperature and a potential explosion.

The FDA has identified the recall of certain devices as a Class I recall, the most serious type of recall. This recall involves removing certain devices from where they are used or sold. This device may cause serious injury or death if you continue to use it. 

For full details, please visit https://www.fda.gov/medical-devices/medical-device-recalls/laryngoscope-recall-medtronic-removes-certain-mcgrath-mac-video-laryngoscopes-updates-use. Any questions, please reply to oems.ambulance@mass.gov.