9601 Documentation Cart With Articulating Arm

Recall Summary A 9601 Documentation Cart with Articulating Arm is being recalled across Canada because it does not meet safety and performance standards for medical devices. The recall affects all units of this cart that were distributed in Canada. This is classified as a Class I recall, which is the most serious classification.

Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2013-01-07
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/a8cf9678-f879-49eb-9fe2-e91a706a9f09