Manufacturer
192 recalls in our database name PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. as the manufacturing or recalling firm.
The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.
Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.
Philips has identified that some Allura Xper FD20 biplane systems may have uninstalled or undocumented drip trays beneath the cooling unit, creating risk for coolant to contact electrical components and cause system shutdown.
A drip tray beneath the cooling unit in some Philips Allura imaging systems was not installed or not adequately documented, potentially allowing coolant to contact electrical components and cause system shutdown.
Philips is recalling 22 Allura Xper imaging systems because the drip tray beneath the cooling unit may not be installed or properly documented. Without it, coolant could contact electrical components and cause system shutdown.
Philips is recalling the Allura Xper FD10 because the drip tray beneath the cooling unit may not be installed in some units, potentially allowing coolant to contact electrical components and cause system shutdown.
Philips is recalling 38 Allura Xper FD10C medical imaging systems in which the cooling unit drip tray may not be properly installed, potentially allowing coolant to contact electrical components and cause system shutdown.
Philips is recalling Azurion diagnostic imaging systems with software versions R2.1.10 and R2.2.10 due to six software defects that may cause system restarts, storage issues, and positioning errors. Approximately 10,466 units distributed worldwide are affected.
In limited Allura Xper FD20 X-ray systems, the cooling unit drip tray was not installed or inadequately documented. This creates a potential for coolant to contact electrical components and trigger system shutdown.
Philips is recalling select Allura Xper FD20/20 imaging systems where the cooling unit drip tray may not be installed. If not installed, coolant could contact electrical components and cause system shutdown.
Philips Azurion 7M20 X-ray imaging systems may experience inconsistent or unavailable motorized movement on the ceiling-mounted FlexArm arm due to bearing lubrication failure affecting 172 units.
Philips Zenition 50 x-ray systems may experience loss of imaging functionality or poor image quality due to corrosion of the Image Intensifier Television control board. Twenty-nine units were affected across multiple U.S. and international locations.
The BIOS battery in Philips Allura Xper FD20 operating room tables may deplete faster than expected, preventing system startup. No warning messages appear before depletion.
Philips recalled 5 Allura Xper FD20/20 OR tables because the BIOS battery depletes faster than designed, preventing the system from starting. No user warnings appear before the battery fails.
The Allura Xper CV20 device may fail to start if the BIOS battery depletes faster than expected. No warning message is shown before the battery becomes low or depleted.
Philips Allura Xper FD20 Biplane medical imaging devices may have BIOS batteries that deplete faster than expected, preventing startup without warning to operators.
The Allura Xper FD10 OR Table may experience faster-than-expected BIOS battery depletion without warning, preventing system startup.
The Allura Xper FD10C cardiac imaging system may fail to start due to faster-than-expected BIOS battery depletion. No warning message appears before battery failure.
Philips Cardio Vascular-Allura Centron cardiac imaging systems may have accelerated BIOS battery depletion that prevents the device from starting. Affected facilities should contact the manufacturer for battery replacement guidance.
Philips Allura Xper FD20/20 fluoroscopy systems may experience premature BIOS battery depletion, preventing system startup without prior warning. 115 units distributed worldwide are affected.
Philips Allura Xper FD20/15 imaging systems are recalled because BIOS batteries may deplete faster than expected, preventing system startup. No warning messages appear before battery failure occurs.
Philips is recalling Allura Xper FD10 imaging systems due to faster-than-expected BIOS battery depletion. When depleted, the system will not start, and no warning appears before battery failure.
Philips is recalling certain Allura Xper FD20/15 OR Tables because the BIOS battery may deplete faster than expected, preventing the system from starting without warning. No user warnings appear before the battery becomes depleted.
Philips Allura Xper FD20 operating room tables have BIOS batteries that may deplete faster than designed, preventing system startup without user warning.
Philips Allura Xper FD20/10 fluoroscopy systems may fail to start if the BIOS battery depletes faster than designed. No warning is given before failure occurs.
Philips Allura Xper FD20 fluoroscopy systems may experience premature BIOS battery depletion, causing unexpected system startup failures. No warning messages alert users before battery depletion.
The BIOS battery in affected Philips Allura Xper FD10/10 fluoroscopy systems may deplete faster than expected, preventing system startup. No warning messages alert users before the battery runs low.