Interventional Fluoroscopic X-ray System
Philips Medical Systems Nederland B.v.'s record for this product code
Recent MDR events
28,862 adverse event reports on file
- Allura Xper FDJul 31, 2026Malfunction3042175844-2026-001967
- Allura Xper FDJul 31, 2026Malfunction3042175844-2026-001969
- Allura Xper FD20Jul 31, 2026Malfunction3042175844-2026-001970
- Allura Xper FDJul 31, 2026Malfunction3042175844-2026-001971
- Allura Xper FD20Jul 31, 2026Malfunction3042175844-2026-001974
- Allura Xper FDJul 31, 2026Malfunction3042175844-2026-001972
- AzurionJul 31, 2026Malfunction3042175844-2026-001975
- AzurionJul 31, 2026Malfunction3042175844-2026-001973
- AzurionJul 31, 2026Malfunction3042175844-2026-001977
- AzurionJul 31, 2026Malfunction3042175844-2026-001978
Recalls
185 recall events for this product code
- Open, ClassifiedAug 10, 2026
Firmware issue potentially leading to loss of geometry movements.
View FDA record ↗ - Open, ClassifiedAug 10, 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 inappropriate treatment and 2) Potential loss of geometry movements that may lead to delay of therapy and procedural complications
View FDA record ↗ - Open, ClassifiedAug 10, 2026
Two software related issues affecting Philips Azurion R3.0 and R3.1 systems: 1) Potential image quality degradation that may lead to delay of therapy, procedural complications and/or inappropriate treatment and 2) Potential loss of geometry movements that may lead to delay of therapy and procedural complications.
View FDA record ↗ - Open, ClassifiedAug 5, 2026
Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.
View FDA record ↗ - Open, ClassifiedAug 5, 2026
Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.
View FDA record ↗ - Open, ClassifiedAug 5, 2026
Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.
View FDA record ↗ - Open, ClassifiedJun 16, 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 additional contrast injection
View FDA record ↗ - Open, ClassifiedJun 1, 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 touching the footswitch pedal without generating an Xray image). The pedal tap may cause a dark image with the next fluoroscopy run.
View FDA record ↗ - Open, ClassifiedJun 1, 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 touching the footswitch pedal without generating an Xray image). The pedal tap may cause a dark image with the next fluoroscopy run.
View FDA record ↗ - Open, ClassifiedJun 1, 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 touching the footswitch pedal without generating an Xray image). The pedal tap may cause a dark image with the next fluoroscopy run.
View FDA record ↗
510(k) clearances
29 clearances for this product code
- K254205Aug 7, 2026
Zenition 30
- K232420Feb 16, 2024
Zenition 30
- K212813Oct 1, 2021
Zenition 70
- K201583Feb 9, 2021
SmartCT R1.0
- K200917May 1, 2020
Azurion R2.1
- K183101Dec 31, 2018
Zenition 50
- K183040Dec 6, 2018
Zenition 70
- K181830Aug 2, 2018
Azurion R2.0
- K172822Nov 22, 2017
Azurion series R1.2
- K172307Oct 24, 2017
Dynamic Coronary Roadmap 2.0