Neoprobe Gamma Detection Device (2019-03-17)

NeoProbe Gamma Detection Device Recall The NeoProbe Gamma Detection Device has been recalled across Canada. The device was recalled due to issues classified as a Class I medical device concern. This recall affects NeoProbe Gamma Detection Devices distributed throughout Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2019-04-29
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/b78ff65d-7a75-4cb6-bad5-34931975d011