AneurysmFlow
This recall involves AneurysmFlow, a medical device used in aneurysm treatment. It's being recalled because the 'mafa ra...
All product recalls associated with Philips Medical Systems Nederland B.V. in Canada, sourced from Health Canada, Transport Canada, and the CFIA.
This recall involves AneurysmFlow, a medical device used in aneurysm treatment. It's being recalled because the 'mafa ra...
This recall involves Philips Allura Xper and Azurion Systems sold in Canada. They are being recalled because the X-ray i...
This recall involves Philips Allura Xper and Allura CV20 Systems used in Canada. They are being recalled because a missi...
This recall involves Azurion R2.1.10 and R2.2.10 systems sold in Canada. They are being recalled because of performance
This recall involves Philips Diagnostic X-Ray Systems sold in Canada. They are being recalled because some ceiling suspe...
This recall involves the Zenition 50 medical device sold in Canada. It's being recalled because of a performance issue d...
This recall involves Allura Xper Systems medical devices sold in Canada. They are being recalled because the BIOS batter...
This recall involves Philips Allura and Azurion Systems sold in Canada. They are being recalled because a component in t...
This recall involves Allura Xper Systems medical devices sold in Canada. They are being recalled because a missing compo...
This recall involves Philips Achieva and Ingenia MRI Systems sold in Canada. They are being recalled because a component...
This recall involves Allura Systems medical devices sold in Canada by Philips Medical Systems Nederland B.V. It's being
This recall involves the Azurion 7 M20 medical device. It's being recalled because bolts connecting the gearbox to the c...
This recall involves Azurion 7 Systems sold in Canada. It's being recalled because of a software issue that may affect s...
This recall involves Philips Achieva and Intera 1.5T MRI Systems. They are being recalled because a component failure co...
This recall involves Philips CT Big Bore systems used in healthcare settings in Canada. They are being recalled because
This recall involves patient tables of Philips Allura and Azurion systems sold in Canada. They are being recalled becaus...
This recall involves Azurion and Allura Systems medical devices sold in Canada. They are being recalled because a finger...
This recall involves Philips Breast Coils used in medical settings in Canada. It's being recalled because a performance
This recall involves Philips Azurion and Allura Systems sold in Canada. They are being recalled because bolts supporting...
This recall involves Philips Allura Xper medical devices sold in Canada. It's being recalled because potential safety is...