Health product recall

Azurion Systems

Last updated

Summary

Product
Azurion Systems
Issue
Medical devices - Performance
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products Lot or serial number Model or catalogue number
Azurion 7 M12 Not applicable. 722 078
Azurion 7 B12 Not applicable. 722 067
Azurion 7 M20 Not applicable. 722 224
Azurion 7 M20 Not applicable. 722 079

Issue

Philips has identified that the float tabletop control on the control module of Azurion systems may experience mechanical wear over time.

The float tabletop control is located on the control module at the table-side. When the control is actuated, the table brakes disengage, allowing adjustment of the longitudinal or transverse position of the table.

Over time, mechanical wear may lead to detachment, cracking, or breakage of the float tabletop control, which may lead to reduced availability or unavailability of longitudinal and transverse tabletop movement, as well as the formation of sharp edges.

Additional information

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

Philips Medical Systems Nederland B.V.

Veenpluis 6, Best, Netherlands, 5684 PC

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Recall date
Identification number
RA-82045

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