FDA Announces Class I Recall of BMC Medical Luna G3 APAP Devices Due to Firmware Defect

The FDA has classified a recall of 20,160 Luna G3 APAP (Model LG3600) devices by BMC Medical Co., Ltd. as Class I, the most serious type of recall. The devices contain a firmware defect (version G3-2.00.76) that could lead to serious adverse health consequences.