Philips North America

Frequent Recalls

19

Recalls

0

Units Recalled

0

Injuries

0

Deaths

1 category · 2026-05-06 to 2026-05-06

Date	Source	Product	Brand	Severity	Units
2026-05-06	FDA Device	FDA Recall: Philips SmartPath to dStream for 1.5T with MR Elastography (MRE). 1. Model Number (REF): 781260.	Philips North America	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Philips Upgrade to MR 7700 with MR Elastography (MRE). 1. Model Number (REF): 782130.	Philips North America	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Philips Ingenia Ambition X with MR Elastography (MRE). 1. Model Number (REF): 781356. 2. Mod	Philips North America	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Philips SmartPath to dStream for 3.0T with MR Elastography (MRE). 1. Model Number (REF): 782145.	Philips North America	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Philips SmartPath to Ingenia Elition X with MR Elastography (MRE). 1. Model Number (REF): 782118	Philips North America	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Philips Ingenia 3.0T with MR Elastography (MRE). 1. Model Number (REF): 781342. 2. Model Num	Philips North America	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Philips Evolution upgrade 3.0T with MR Elastography (MRE). 1. Model Number (REF): 782143. 2.	Philips North America	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Philips Ingenia Ambition S with MR Elastography (MRE). 1. Model Number (REF): 781359. 2. Mod	Philips North America	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Philips Achieva 1.5T with MR Elastography (MRE). 1. Model Number (REF): 781196. 2. Model Numb	Philips North America	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Philips Ingenia 1.5T CX with MR Elastography (MRE). 1. Model Number (REF): 781262.	Philips North America	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Philips Ingenia Elition S with MR Elastography (MRE). 1. Model Number (REF): 781357. 2. Mode	Philips North America	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Philips Ingenia Elition X with MR Elastography (MRE). 1. Model Number (REF): 781358. 2. Mode	Philips North America	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Philips Ingenia 3.0T CX with MR Elastography (MRE). 1. Model Number (REF): 781271. 2. Model	Philips North America	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Philips Achieva 1.5T Initial system with MR Elastography (MRE). 1. Model Number (REF): 781178.	Philips North America	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Philips MR 7700 with MR Elastography (MRE). 1. Model Number (REF): 782120. 2. Model Number (	Philips North America	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Philips Achieva 3.0T with MR Elastography (MRE). 1. Model Number (REF): 781278.	Philips North America	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Philips Evolution Upgrade 1.5T with MR Elastography (MRE). 1. Model Number (REF): 782116 2. M	Philips North America	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Philips Ingenia 1.5T with MR Elastography (MRE). 1. Model Number (REF): 781315. 2. Model Num	Philips North America	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Philips SmartPath to dStream for XR and 3.0T with MR Elastography (MRE). 1. Model Number (REF):	Philips North America	Class II	N/A