Health product recall

O-Arm 1000 Imaging System - Base O-Arm

Last updated

Summary

Product
O-Arm 1000 Imaging System - Base O-Arm
Issue
Medical devices - Labelling and packaging
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products Lot or serial number Model or catalog number
O-Arm 1000 Imaging System - Base O-Arm C2968 C3363 BI-700-00027120

Issue

Medtronic identified O-Arm O2 imaging systems where an internal ground cable may be installed backward. When the cable is installed inverted, a portion of the uninsulated cable is not covered by the zippered jacket.

Recall start date: July 25, 2023

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Radiology
Companies

Medtronic Navigation, Inc. (Littleton)

300 Foster Street, Littleton, Massachusetts, United States, 01460

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-74066