Health & Personal Care
HIGH
FDA DEVICE
Philips Recalls Allura Xper FD10C Systems Over Electrical Hazard
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Recalls
75 recalls found for PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.. Check current safety alerts and related brands before using affected products.
- Active recalls
- 75
- Pages
- 4
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Device Recalled Due to Electrical Hazard
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips has
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Recalls Allura Xper FD20 Over Electrical Hazard
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips has
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Imaging System Recalled Over Electrical Hazard
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips has
Health & Personal Care
HIGH
FDA DEVICE
Philips Recalls Azurion Systems Over Software Issues
Philips recalled 10,466 Azurion Systems on December 12, 2025, due to six software issues that can cause system failures. Users must stop using the devices immediately. The recall affects models sold worldwide, including in the U.S.
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Six (6)
Health & Personal Care
HIGH
FDA DEVICE
Philips Azurion System Recalled Due to Software Malfunction
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips has
Health & Personal Care
HIGH
FDA DEVICE
Philips Azurion Systems Recalled Due to Software Issues
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Nine (9)
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Nederland 718096 Zenition 50 Interventional X-Ray System Recalled in 2025
Over time some systems may experience loss of imaging functionality and/or poor image quality due to potential corrosion of the Image Intensifier Television (IITV) control board.
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Over time
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD20 Biplane OR Table Recall Affects 5 Units Worldwide (2025)
Philips Medical Systems Nederland B.V.
Systems may
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD20/10 Recall 45 Units Worldwide in 2025
Philips Medical Systems Nederland B.V.
Systems may
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD10/10 Recall for 286 Units Worldwide in 2025
Philips Medical Systems Nederland B.V.
Systems may
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Nederland B.V. Recalled 98 Imaging Systems for CMOS Battery, HDD, PSU Deteri
Philips Medical Systems Nederland B.V.
Systems may
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD10 OR Table Recall for 2 Units Worldwide in 2025
Philips Medical Systems Nederland B.V.
Systems may
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Nederland B.V. Allura CV20 Recalled in Global Distribution for Component D-7
Philips Medical Systems Nederland B.V.
Systems may
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD20/20 Recall Affects 75 Systems Worldwide for Internal Component Deterioration
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Systems may
Health & Personal Care
HIGH
FDA DEVICE
PHILIPS Allura Xper FD10/10 Recall Tied to BIOS Battery Depletion
Philips Medical Systems Nederland B.V.
The BIOS
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD10 OR Table 722033 Recall 2 Units Worldwide (2025)
Philips Medical Systems Nederland B.V.
The BIOS
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Nederland Faces High-Risk Recall for Allura Xper FD20/15 BIOS Battery
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
The BIOS
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Recalls 87 BIOS Battery Models After Start-up Failure Risk
Philips Medical Systems Nederland B.V.
The BIOS
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Nederland recalls 5 Allura Xper FD20/20 OR Tables for BIOS battery startup
Philips Medical Systems Nederland B.V.
The BIOS
Brand Statistics
Total Recalls
75
Pages
4