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.
The Philips Allura Xper FD20/15 X-ray imaging system may fail to initiate or may initiate intermittently when using the wired foot switch. Philips is recalling 296 affected units (68 in the US, 228 internationally) to address this functional defect.
The Azurion 7 M12 X-ray imaging system may fail to initiate imaging or may operate intermittently due to a wired foot switch malfunction. No patient injuries have been reported.
The Philips ALLURA Xper FD10/10 X-ray system may fail to initiate or operate intermittently when using its wired foot switch. Approximately 112 affected units have been distributed in the United States and internationally.
Philips has identified a foot switch defect in Azurion 7 M20 X-ray systems that may prevent imaging initiation or cause intermittent imaging operation. Approximately 5,167 units are affected worldwide, including 1,728 in the U.S.
Philips is recalling the ALLURA Xper FD20 Biplane OR Table due to a wired foot switch malfunction that may prevent X-ray imaging from being initiated or cause it to operate intermittently.
Philips ALLURA Xper FD20 X-ray systems may fail to initiate imaging or operate intermittently when using the wired foot switch. Affected medical facilities should contact Philips for service evaluation.
Philips Azurion 7 B20 fluoroscopy systems may move unexpectedly when the Reset Geometry button is pressed, even with the table lock engaged, creating a potential safety risk during medical procedures.
Philips is recalling the Azurion 7 M20 imaging system because the patient table may move unexpectedly when the Reset Geometry button is pressed, even when the table lock is engaged. Approximately 5,136 units are affected worldwide.
Philips Azurion 3 M12 fluoroscopy systems may experience unexpected table movement when the Reset Geometry button is pressed, even when the table lock is active. The recall affects 291 units distributed worldwide.
Philips Azurion 5 M12 imaging system tables may move unexpectedly when the Reset Geometry button is pressed, even when the table lock is active, posing a safety risk during medical procedures.
Philips is recalling the Azurion 3 M15 imaging system because the patient table may move unexpectedly when the Reset Geometry button is pressed, even when locked. This poses a patient safety hazard during interventional procedures.
Philips has recalled the Azurion 7 M12 imaging system because the examination table may move unexpectedly when the Reset Geometry button is pressed, even if the table lock is active. This could pose a patient safety risk.
Philips is recalling 922 Azurion 5 M20 fluoroscopy systems because the patient table may move unexpectedly when the Reset Geometry button is pressed, even when the table lock is active.
The Philips Azurion 7 B12 medical imaging system may experience unexpected table movement when the Reset Geometry button is pressed, even if the table lock is engaged. This could affect patient safety during medical procedures.
Philips has recalled the Azurion imaging system (Software Version R3.1) in 228 units worldwide due to two software issues that may cause loss of imaging functionality, motorized movement, incorrect image content, or data loss.
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 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.
The Philips Allura Xper FD20 fluoroscopy system may lack a drip tray beneath its cooling unit, potentially allowing coolant to contact electrical components and cause device shutdown. The recall affects 143 units worldwide.
Certain Philips Allura Xper diagnostic imaging systems may be missing a cooling unit drip tray, which could allow coolant to contact electrical components and trigger system shutdown.
Philips is recalling 12 Allura Xper FD10F angiography systems worldwide because the cooling system's drip tray may not be installed. Without the tray, coolant could contact electrical components and cause short-circuits leading to system shutdown.
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.
Certain Philips Allura Xper FD20/10 imaging systems may lack a required drip tray beneath the cooling unit. If missing, coolant could contact electrical components and cause system shutdown.
Philips is recalling Allura Xper FD10 X-ray systems with potentially missing drip trays beneath the cooling unit. If missing, coolant could contact electrical components, causing short-circuits and system shutdown.
Two Philips Allura Xper FD20 X-ray systems may lack proper installation of the cooling unit drip tray, risking coolant leakage onto electrical components and potential equipment 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.