Bd Max System (2018-10-03)

BD MAX System Recall Summary The BD MAX System, a medical device, is being recalled across Canada due to a safety or effectiveness issue. This recall affects all BD MAX System devices that were distributed in Canada. The FDA has classified this as a Class I recall, which is the most serious classification.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2018-10-26
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/69e3eeb7-8139-463f-a6a9-733d1ee0b26e