Juno Drf (2019-11-14)

Juno DRF Recall Summary Juno DRF, a medical device, has been recalled across Canada due to a Class I safety issue. The specific reason for the recall relates to problems with the device itself, though the exact nature is not detailed in the available information. This recall affects all Juno DRF devices distributed in Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2019-11-29
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/6871f522-05aa-433a-8f92-21f1100f3791