PHILIPS MEDICAL SYSTEMS Recalls

4 recalls found for PHILIPS MEDICAL SYSTEMS. Check if any of your products are affected.

HIGH
FDA DEVICE

Philips Spectral CT on Rails. Model Number: 728334.

Philips has identified three software issues: 1. During a continuous CT (CCT) scan, there is the potential that the Gantry could remain at the current scan position after pressing Go. 2. Potential where the message of Previous Surview Exists Select Previous Surview? <Yes> or <No> should display but does not appear. 3. After performing Surview and planning the Brain Helical acquisition by setting Brain Area DoseRight Index to increase the dose, there is the potential that the Define Head Area option in the context menu is grayed out.

PHILIPS MEDICAL SYSTEMS
Philips has
Read more
Health & Personal Care
HIGH
FDA DEVICE

Philips Allura Xper FD20 Biplane Recall Affects 268 Units Worldwide (2025)

Philips Medical Systems Nederland B.V. recalled 268 Allura Xper FD20 Biplane imaging systems worldwide, including 102 in the United States. The recall cites deterioration of internal components that could disable motorized movements. Hospitals should stop using the devices immediately and follow the manufacturer’s recall instructions.

Philips Medical Systems
Systems may
Read more
Health & Personal Care
HIGH
FDA DEVICE

Philips Allura Xper FD20 Recall Affects 2,114 Units Globally Over Power Component Deterioration

Philips Medical Systems Nederland B.V. recalls 2,114 Allura Xper FD20 imaging systems sold worldwide after reports that internal components may deteriorate. The recall covers models 722012, 722028 and 722006 with associated 510(k) numbers K102005 and K130842, K130638, K133292, K141979, K161563, K162859, K033737, K041949. If deterioration occurs, motorized movements may fail. Manual and imaging功能s,

Philips Medical Systems
Systems may
Read more
Health & Personal Care
HIGH
FDA DEVICE

Philips Pinnacle3 Recall: 810 Units Over ROI Image Error in 2025

Philips Medical Systems recalled 810 Pinnacle Radiation Therapy Planning System units nationwide to healthcare providers. A software issue may cause an image error of the Region of Interest for HFP, FFS, and FFP orientations. Hospitals and clinics should stop using the software immediately and follow the manufacturer’s instructions.

Philips Medical Systems
Due to
Read more

Brand Statistics

Total Recalls
4
Pages
1

Related Brands

GLYCOPYRROLATEZimmer SurgicalEthicon Endo-SurgeryStuffed FoodsStryker Sustainability SolutionsBlue WaveAisstxoerMeridian Bioscience