PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Recalls

Allura system; System Code Description (Model Numbers): Allura Xper FD10 (722003, 722010, 722026), Allura Xper FD10 OR Table (722022, 722033), Allura Xper FD10/10 (722005, 722011, 722027), Allura...

Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063, 722221), Azurion 3 M15 (722064, 722222), Azurion 5 M12 (722227), Azurion 5 M20 (722228), Azurion 7 B12 (722067,...

Integris-Allura system; System Code Description (Model Numbers): Integris CV Cesar-Powerpack-Visub-Nicol (722030), Integris Allura 15 & 12 (monoplane) (722043), INTEGRIS Allura 15-12 (biplane)...

Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063), Azurion 3 M15 (722064), Azurion 7 B12 (722067), Azurion 7 B20 (722068), Azurion 7 M12 (722078), Azurion 7 M20 (722079,...

Philips Azurion systems not configured with an optional auxiliary pan handle. Includes the below product descriptions and corresponding model numbers. 1. Azurion 3 M12; Model Numbers: 722063,...

Potential safety issue with Philips Azurion systems, where longitudinal and transverse table movements may be impacted due to mechanical wear of the Float Tabletop control on the control module.

Allura system; System Code Description (Model Numbers): Allura Xper FD10C (722001), Allura Xper FD10F (722002), Allura Xper FD10 (722003, 722010, 722026), Allura Xper FD10/10 (722005, 722011,...

Philips Azurion. System Code Description (Model Number): Azurion 3 M12 (722221, 722229), Azurion 3 M15 (722222, 722230), Azurion 5 (722281), Azurion 5 M12 (722227, 722231), Azurion 5 M20 (722228,...

Potential for the bolts and plastic parts of the Cable Hose Carriers that hold the cable hose to the monitor ceiling suspension may loosen and/or break over time due to the forces applied when the monitor is moved or rotated.

Philips AneurysmFlow. Model Number: 001015. AneurysmFlow is a software medical device (Interventional Tool) intended to be used in combination with a Philips interventional X-ray system and 3DRA...

Philips Vue Motion V12 Recall for 3,552 Units Over Cine Frame Sequencing Error (2026)

Potential that mis-ordered frames in Vue Motion during dynamic cine runs may cause images frames to display out of sequence.

Philips Azurion 3 M12 Recall for Intermittent X-ray Imaging (298 Units Worldwide, 2026)

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

Philips Allura Xper FD10C X-ray System Recall for 15 Units Worldwide (2026)

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

Philips Azurion 5 M12 X-ray System Recall 2026: 345 Worldwide Units Affected

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

Philips ALLURA Xper FD20 Recall for 5,084 Units Over Intermittent X-ray Imaging (2026)

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

Philips Allura Xper FD10F Recall for 10 Units Worldwide (2026)

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

Philips Medical Systems Nederland recall 296 Allura Xper FD20/15 Imaging Systems Over Foot Switch Fl

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

Philips ALLURA Xper FD10/10 Imaging System Recalled for Intermittent X-ray Activation (112 Units)

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

Philips Allura Xper FD20/20 Recall 111 Systems Worldwide Over Intermittent Imaging (2026)

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

Philips Azurion 5 M20 Recall: 920 Imaging Systems Worldwide Affected (2026)

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

Philips ALLURA Xper FD20 OR Table Recalled Worldwide; 196 Units Affected (2026)

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

Philips ALLURA Xper FD10 OR Table Recalled for Intermittent X-ray Activation (2 Units, 2026)

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.