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Arjohuntleigh Magog recalls ARJOHUNTLEIGH GETINGE GROUP, RotoProne Therapy System, Model Number 209800
Recalled February 13, 2019 · FDA recall Z-0802-2019 · Arjohuntleigh Magog
Hazard
Inability or difficulty in unbuckling/releasing the proning arm buckle might delay patient access in an emergency situation such as cardiac arrest. This, in turn, could contribute to a life-threatening event. · FDA Class II
Units
231 units
Sold at
US, Saudi Arabia, and Kuwait
Description
Inability or difficulty in unbuckling/releasing the proning arm buckle might delay patient access in an emergency situation such as cardiac arrest. This, in turn, could contribute to a life-threatening event.
Product
ARJOHUNTLEIGH GETINGE GROUP, RotoProne Therapy System, Model Number 209800
Manufacturer(s)
Arjohuntleigh Magog
Made in
Canada
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →