Lunar Idxa (2020-04-14)

Lunar iDXA Recall Summary GE Healthcare's Lunar iDXA bone density scanning equipment has been recalled across Canada due to a defect in the device's software that could cause inaccurate measurement results. The recall affects all Lunar iDXA systems distributed in Canada. This is classified as a Class I recall, meaning the device poses a serious risk to patient health.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2020-05-08

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/1d21bd27-5745-472d-a116-1a5caddf8bea