Microfuge 20r 120 V 60 Hz With Fa241.5p Ivd (2016-03-08)

Recall Summary Eppendorf is recalling the MICROFUGE 20R 120V 60Hz centrifuge with FA241.5P rotor across Canada because it has been classified as a Class I medical device recall. The specific reason for the recall relates to its status as an in vitro diagnostic (IVD) device, though detailed technical reasons are not specified in this notice.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2016-03-29
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/2382624e-f9fc-4935-8354-3860d92e7ff6