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KaVo Dental Technologies LLC recalls cone-beam CT system
Recalled May 1, 2019 · FDA recall Z-1101-2019 · KaVo Dental Technologies
Hazard
ORTHOPANTOMOGRAPH OP 3D device has a defect in the device firmware versions 2.1.0 and 2.1.1 · FDA Class II
Units
230
Sold at
US distribution in NC
Description
ORTHOPANTOMOGRAPH OP 3D device has a defect in the device firmware versions 2.1.0 and 2.1.1
Product
cone-beam CT system
Manufacturer(s)
KaVo Dental Technologies LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →