Philips Medical Systems Nederland B.v. recalls
108 recalls filed under Philips Medical Systems Nederland B.v.. The most recent was published August 19, 2026.
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Class II · 2 months ago
Philips Azurion Rystem, Model Numbers: 722063, 722064, 722067 recall: Two software related issues affecting Azurion R2.2.10 Systems: 1) Potential
Two software related issues affecting Azurion R2.2.10 Systems: 1) Potential image quality degradation that may lead to delay of therapy, procedural…
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Class II · 2 months ago
Philips Azurion, Model Numbers: 722229, 722230, 722231, 722232 recall: Two software related issues: 1) Potential image quality degradation
Two software related issues: 1) Potential image quality degradation that may lead to delay of therapy, procedural complications and/or inappropriate…
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Class II · 2 months ago
Philips Medical Systems Nederland B.v. Allura Xper FD. Model Numbers: 722026 recall: Firmware issue potentially leading to loss of geometry movements
Firmware issue potentially leading to loss of geometry movements.
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Class II · 2 months ago
Philips Allura under the following System Descriptions recall: Potential Loss of imaging functionality, loss of motorized movement
Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.
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Class II · 2 months ago
Philips Azurion under the following System Descriptions recall: Potential Loss of imaging functionality, loss of motorized movement
Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.
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Class II · 2 months ago
Philips Allura, Cardio Vascular-Allura Centron recall: Potential Loss of imaging functionality, loss of motorized movement
Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.
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Class II · 4 months ago
Philips Allura Xper with the following Model Numbers: Model # 722001 recall: Philips Allura Xper and MultiDiagnost-Eleva systems Hand switch button
Philips Allura Xper and MultiDiagnost-Eleva systems Hand switch button not fully releasing potentially leading to loss of imaging functionality or…
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Class II · 4 months ago
Philips MultiDiagnost Eleva with the following Model Numbers: Model # recall: Philips Allura Xper and MultiDiagnost-Eleva systems Hand switch button
Philips Allura Xper and MultiDiagnost-Eleva systems Hand switch button not fully releasing potentially leading to loss of imaging functionality or…
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Class II · 5 months ago
Philips Azurion 5M12, Model Numbers: 722227 with Software release recall: During the device phase of Roadmap Pro, a user may experience a dark image
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…
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Class II · 5 months ago
Philips Azurion 7B20/15, Model Numbers: 722068 recall: During the device phase of Roadmap Pro, a user may experience a dark image
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…
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Class II · 5 months ago
Philips Azurion 7M20, Model Numbers: 722079 recall: During the device phase of Roadmap Pro, a user may experience a dark image
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…
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Class II · 5 months ago
Philips Azurion 5M20, Model Numbers: 722228 with Software release recall: During the device phase of Roadmap Pro, a user may experience a dark image
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…
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Class II · 5 months ago
Philips Azurion 7M12, Model Numbers: 722078 recall: During the device phase of Roadmap Pro, a user may experience a dark image
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…
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Class II · 5 months ago
Philips Azurion 7B12/12, Model Numbers: 722067 recall: During the device phase of Roadmap Pro, a user may experience a dark image
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…
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Class II · 5 months ago
Philips Azurion 3M12, Model Numbers: 722063 recall: During the device phase of Roadmap Pro, a user may experience a dark image
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…
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Class II · 5 months ago
Philips Azurion 3M15, Model Numbers: 722064 recall: During the device phase of Roadmap Pro, a user may experience a dark image
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…
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Class II · 5 months ago
Philips Medical Systems Nederland B.v. Allura system recall: It was identified that HDDs used in the PCs of Azurion and Allura systems
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…
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Class II · 5 months ago
Philips Medical Systems Nederland B.v. Azurion system recall: It was identified that HDDs used in the PCs of Azurion and Allura systems
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…
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Class II · 5 months ago
Philips Medical Systems Nederland B.v. Allura system recall: The deaeration hose in X-ray tube cooling units type CU3101
The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially…
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Class II · 5 months ago
Philips Medical Systems Nederland B.v. Integris-Allura system recall: The deaeration hose in X-ray tube cooling units type CU3101
The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially…
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Class II · 5 months ago
Philips Azurion systems not configured with an optional auxiliary pan recall: Potential safety issue with Philips Azurion systems
Potential safety issue with Philips Azurion systems, where longitudinal and transverse table movements may be impacted due to mechanical wear of the…
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Class II · 5 months ago
Philips Medical Systems Nederland B.v. Azurion system recall: The deaeration hose in X-ray tube cooling units type CU3101
The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially…
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Class II · 5 months ago
Philips Azurion. System Code Description : Azurion 3 M12 recall: Potential for the bolts and plastic parts of the Cable Hose Carriers
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…
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Class II · 6 months ago
Philips AneurysmFlow recall: Potential safety issue involving the Mean Aneurysm Flow Amplitude (MAFA)
Potential safety issue involving the Mean Aneurysm Flow Amplitude (MAFA) ratio of AneurysmFlow (Interventional Tool). Philips has determined that the…
About this page
Philips Medical Systems Nederland B.v. appears here because a federal agency named it as the recalling firm or the brand on the label. A recall is not a judgement about everything the company sells — it covers only the lot codes and models listed in each notice.