PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
23 recent recalls on record for PHILIPS MEDICAL SYSTEMS NEDERLAND B.V in connected official government data as of September 7, 2026 at 6:00 AM UTC.
Models with recalls
All PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
FDA Class II · Medical device · August 19, 2026
Two software related issues: 1) Potential image quality degradation that may lead to delay of therapy, procedural complications and/or inappropriate treatment and 2) Potential loss…
Official ID Z-2932-2026 ·
Official record ↗
FDA Class II · Medical device · August 19, 2026
Two software related issues affecting Azurion R2.2.10 Systems: 1) Potential image quality degradation that may lead to delay of therapy, procedural complications and/or inappropria…
Official ID Z-2931-2026 ·
Official record ↗
FDA Class II · Medical device · August 19, 2026
Firmware issue potentially leading to loss of geometry movements.
Official ID Z-2928-2026 ·
Official record ↗
FDA Class II · Medical device · August 12, 2026
Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.
Official ID Z-2893-2026 ·
Official record ↗
FDA Class II · Medical device · August 12, 2026
Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.
Official ID Z-2892-2026 ·
Official record ↗
FDA Class II · Medical device · August 12, 2026
Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.
Official ID Z-2891-2026 ·
Official record ↗
FDA Class II · Medical device · June 24, 2026
Philips Allura Xper and MultiDiagnost-Eleva systems Hand switch button not fully releasing potentially leading to loss of imaging functionality or unintended radiation exposure and…
Official ID Z-2412-2026 ·
Official record ↗
FDA Class II · Medical device · June 24, 2026
Philips Allura Xper and MultiDiagnost-Eleva systems Hand switch button not fully releasing potentially leading to loss of imaging functionality or unintended radiation exposure and…
Official ID Z-2411-2026 ·
Official record ↗
FDA Class II · Medical device · June 10, 2026
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly tou…
Official ID Z-2291-2026 ·
Official record ↗
FDA Class II · Medical device · June 10, 2026
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly tou…
Official ID Z-2290-2026 ·
Official record ↗
FDA Class II · Medical device · June 10, 2026
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly tou…
Official ID Z-2289-2026 ·
Official record ↗
FDA Class II · Medical device · June 10, 2026
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly tou…
Official ID Z-2288-2026 ·
Official record ↗
FDA Class II · Medical device · June 10, 2026
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly tou…
Official ID Z-2287-2026 ·
Official record ↗
FDA Class II · Medical device · June 10, 2026
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly tou…
Official ID Z-2286-2026 ·
Official record ↗
FDA Class II · Medical device · June 10, 2026
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly tou…
Official ID Z-2285-2026 ·
Official record ↗
FDA Class II · Medical device · June 10, 2026
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly tou…
Official ID Z-2284-2026 ·
Official record ↗
FDA Class II · Medical device · June 3, 2026
It was identified that HDDs used in the PCs of Azurion and Allura systems may show a decrease in performance as they age, particularly beyond six years of service. Issues with an H…
Official ID Z-2259-2026 ·
Official record ↗
FDA Class II · Medical device · June 3, 2026
It was identified that HDDs used in the PCs of Azurion and Allura systems may show a decrease in performance as they age, particularly beyond six years of service. Issues with an H…
Official ID Z-2258-2026 ·
Official record ↗
FDA Class II · Medical device · May 27, 2026
The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in oil leakage. Oil leaka…
Official ID Z-2229-2026 ·
Official record ↗
FDA Class II · Medical device · May 27, 2026
The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in oil leakage. Oil leaka…
Official ID Z-2228-2026 ·
Official record ↗
FDA Class II · Medical device · May 27, 2026
The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in oil leakage. Oil leaka…
Official ID Z-2227-2026 ·
Official record ↗
FDA Class II · Medical device · May 27, 2026
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 c…
Official ID Z-2225-2026 ·
Official record ↗
FDA Class II · Medical device · May 20, 2026
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 …
Official ID Z-2170-2026 ·
Official record ↗
Compiled from official public-domain government data. Last checked September 7, 2026 at 6:00 AM UTC.