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 |
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
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