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Please note: using the search filters may not provide accurate search results for records prior to November 2021. When searching for older records, please ensure that you use the include archived checkbox.

Displaying 1 - 10 of 10 items.

" " Philips Wired Foot Switch
Philips has become aware of a potential safety issue with the wired foot switch used with the Philips Allura Xper, Allura Centron, Azurion and Multidiagnost‐Eleva systems, where there is a possibility of loss of imaging functionality resulting from no or…
RecallHealth product recall | 2023-08-30
" " Philips Multidiagnost Eleva, Allura Xper and Azurion systems
Philips has become aware of a potential safety issue with the wired and wireless foot switch used with the Philips Multidiagnost Eleva, Allura Xper and Azurion systems, where there is a possibility of unintended radiation. The wired and wireless foot…
RecallHealth product recall | 2023-08-21
" " Philips Allura Xper and Azurion 7 Systems
Philips has become aware of several situations that can result in a loss of availability of the wireless foot switch during a procedure. Identified issues that may result in the wireless foot switch not being available are: • Loss of bluetooth…
RecallHealth product recall | 2023-07-13
" " Philips Azurion and Allura Systems
Due to the forces applied during the movement of the C-arc of the Azurion and Allura systems, the bolts supporting the flexmove carriage may become loose and/or break, and cracks may appear in the flexmove carriage. Recall start date : June 12, 2023
RecallHealth product recall | 2023-06-22
" " Philips Azurion System
Philips Azurion System may unexpectedly lose X-ray functionality. Due to a software issue, a mechanism that is present in the system to manage the number and size of log trace files does not function properly. Without this mechanism, the log trace files…
RecallHealth product recall | 2023-03-31
" " Smartperfusion and 2D perfusion
Philips has identified through an internal investigation that Smartperfusion and 2D perfusion have technical issues related to the way the perfusion signal is generated and processed, which may lead to inaccurate presentations of time density curves and…
RecallHealth product recall | 2023-03-03
" " 3T MRI Systems
Philips has identified an issue where a specific component failure in the gradient coil of where the affected 3T MR Systems identified above may act as a heat source, with a potential to produce smoke and/or fire.  If the components failure…
RecallHealth product recall | 2022-12-16
" " Allura Xper Fd10 & Fd20 products
Philips has discovered a problem with the flat detector cooling system. Due to a leak in the flat detector cooling system, cooling liquid may leak outside the drip tray of the laird chiller. If this occurs, the liquid may drip into electrical components…
RecallHealth product recall | 2021-12-13
" " ALLURA XPER FD10 and FD20/10 (PRODUCT OF ALLURACLARITY FAMILY)
A problem has been identified in the Philips Allura Xper and Azurion systems that could pose a risk for patients. Philips has discovered that the wireless foot switch can suddenly stop responding due to a firmware bug when a number of ambient conditions…
RecallHealth product recall | 2021-11-25
" " ALLURA XPER and AZURION 7
A problem has been identified in the Philips Allura XPER and Azurion systems that could pose a risk for patients. Philips has discovered that the wireless foot switch can suddenly stop responding due to a firmware bug when a number of…
RecallHealth product recall | 2021-11-12
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