Biopince Automatic Full Core Biopsy Instrument (2019-12-03)

BioPince Automatic Full Core Biopsy Instrument Recall The BioPince Automatic Full Core Biopsy Instrument is being recalled across Canada due to a medical device issue. This device is used to obtain tissue samples for diagnostic purposes. The recall is classified as Class I, meaning there is a serious potential health risk associated with the device.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2019-12-20
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/830e2dff-df5c-46ee-9574-6507c01b15d0