Philips Medical Systems Nederland B.v.
High Tech Campus 36, Eindhoven Noord-Brabant, NL
Registered product codes
8 product codes
Recent MDR events
35,651 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, 2026Malfunction3042175844-2026-001968
- 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
- Allura Xper FDJul 31, 2026Malfunction3042175844-2026-001976
Recalls
209 on file
- 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 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 ↗
Compliance history
Matched by FEI 3000976525.
FDA inspections
1 on file
- Official Action Indicated (OAI)Jan 17, 2025
Compliance: Devices
Inspection citations
0 on file
No citations on file for this FEI number.
Compliance actions
1 on file
Import refusals
0 on file
No import refusals on file for this FEI number.