CanadaPhilips Azurion Systems (models Azurion 7 M12 catalogue 722 078; Azurion 7 B12 catalogue 722 067; Azurion 7 M20 catalogue 722 224; Azurion 7 M20 catalogue 722 079) are affected — the float tabletop control located on the table-side control module may experience mechanical wear. Wear can cause detachment, cracking or breakage, which may reduce or prevent longitudinal and transverse tabletop movement and can create sharp edges. Contact the manufacturer for additional information.
What's being recalled
Companies: Philips Medical Systems Nederland B.V., Veenpluis 6, Best, Netherlands, 5684 PC.
How to identify it
Affected products: Azurion 7 M12; Lot or serial number: Not applicable.; Model or catalogue number: 722 078
Affected products: Azurion 7 B12; Lot or serial number: Not applicable.; Model or catalogue number: 722 067
Affected products: Azurion 7 M20; Lot or serial number: Not applicable.; Model or catalogue number: 722 224
Affected products: Azurion 7 M20; Lot or serial number: Not applicable.; Model or catalogue number: 722 079
The hazard
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.
What to do
Contact the manufacturer if you require additional information.
The official notice
This page is a summary of the notice published by Health Canada, collected from Health Canada, CFIA and Transport Canada. Check the original before you act on it.
Read the official notice (opens in a new tab)