Fresh Recalls

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

Allura Xper FD (1)Allura system (2)Azurion system (2)Integris-Allura system (1)Philips Allura (1)Philips Allura Xper with the following Model Numbers (1)Philips Allura under the following System Descriptions and corresponding model numbers (1)Philips Azurion (2)Philips Azurion 3M12 (1)Philips Azurion 3M15 (1)Philips Azurion 5M12 (1)Philips Azurion 5M20 (1)Philips Azurion 7B12/12 (1)Philips Azurion 7B20/15 (1)Philips Azurion 7M12 (1)Philips Azurion 7M20 (1)Philips Azurion Rystem (1)Philips Azurion systems not configured with an optional auxiliary pan handle (1)Philips Azurion under the following System Descriptions and corresponding model numbers (1)Philips MultiDiagnost Eleva with the following Model Numbers (1)

All PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls

FDA Class II · Medical device · August 19, 2026

Philips Azurion recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

Philips Azurion Rystem recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

Allura Xper FD recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Firmware issue potentially leading to loss of geometry movements.

Official ID Z-2928-2026 · Official record ↗

FDA Class II · Medical device · August 12, 2026

Philips Allura recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

Philips Azurion under the following System Descriptions and corresponding model numbers recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

Philips Allura under the following System Descriptions and corresponding model numbers recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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 with the following Model Numbers recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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 MultiDiagnost Eleva with the following Model Numbers recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

Philips Azurion 7M20 recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

Philips Azurion 7M12 recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

Philips Azurion 7B20/15 recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

Philips Azurion 7B12/12 recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

Philips Azurion 5M20 recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

Philips Azurion 5M12 recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

Philips Azurion 3M15 recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

Philips Azurion 3M12 recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

Allura system recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

Azurion system recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

Integris-Allura system recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

Allura system recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

Azurion system recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

Philips Azurion systems not configured with an optional auxiliary pan handle recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

Philips Azurion recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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 ↗

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Compiled from official public-domain government data. Last checked September 7, 2026 at 6:00 AM UTC.