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O-arm 1000 imaging system - base o-arm
Official notice
4 Aug 2023
Last checked
4 Aug 2023
An official Health Canada notice concerns O-arm 1000 imaging system - base o-arm. 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 Published 2023-08-04.
What to do now
Contact the manufacturer if you require additional information.
Recall number
74066
Official notice
2023-08-04
The hazard
The hazard
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
How to check if you're affected
How to check if you're affected
Compare the product name and identifiers below with the item you own. Follow the official notice if they match.
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Affected products
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Risk / hazard
Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
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Company & contacts
Company & contacts
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Brand: Medtronic Navigation [littleton], O-arm 1000 Imaging System - Base O-arm.
Source & status
Source & status
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Recall details
Recall details
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Documents, notices & source
See the official notice and source documents for full details.
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