Philips North America Recalls

23 recalls on record in the United States

medical: 23
medical Class II
2026-05-06

Philips North America recalls Philips SmartPath to dStream for 3.0T with MR Elastography (

The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.

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medical Class II
2026-05-06

Philips North America recalls Philips SmartPath to Ingenia Elition X with MR Elastography

The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.

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medical Class II
2026-05-06

Philips North America recalls Philips Ingenia 3.0T with MR Elastography (MRE). 1. Mode

The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.

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medical Class II
2026-05-06

Philips North America recalls Philips Evolution upgrade 3.0T with MR Elastography (MRE).

The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.

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medical Class II
2026-05-06

Philips North America recalls Philips Ingenia Ambition S with MR Elastography (MRE). 1

The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.

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medical Class II
2026-05-06

Philips North America recalls Philips Achieva 1.5T with MR Elastography (MRE). 1. Mode

The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.

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medical Class II
2026-05-06

Philips North America recalls Philips Ingenia 1.5T CX with MR Elastography (MRE). 1. M

The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.

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medical Class II
2026-05-06

Philips North America recalls Philips Ingenia Elition X with MR Elastography (MRE). 1.

The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.

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medical Class II
2026-05-06

Philips North America recalls Philips Ingenia 3.0T CX with MR Elastography (MRE). 1. M

The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.

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medical Class II
2026-05-06

Philips North America recalls Philips Achieva 1.5T Initial system with MR Elastography (MR

The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.

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medical Class II
2026-05-06

Philips North America recalls Philips Ingenia 1.5T with MR Elastography (MRE). 1. Mode

The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.

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medical Class II
2026-05-06

Philips North America recalls Philips MR 7700 with MR Elastography (MRE). 1. Model Num

The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.

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medical Class II
2026-05-06

Philips North America recalls Philips Achieva 3.0T with MR Elastography (MRE). 1. Mode

The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.

View recall details →

medical Class II
2026-05-06

Philips North America recalls Philips Evolution Upgrade 1.5T with MR Elastography (MRE).

The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.

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medical Class II
2026-05-06

Philips North America recalls Philips Ingenia Elition S with MR Elastography (MRE). 1.

The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.

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medical Class II
2026-05-06

Philips North America recalls Philips Upgrade to MR 7700 with MR Elastography (MRE). 1

The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.

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medical Class II
2026-05-06

Philips North America recalls Philips Ingenia Ambition X with MR Elastography (MRE). 1

The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.

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medical Class II
2026-05-06

Philips North America recalls Philips SmartPath to dStream for XR and 3.0T with MR Elastog

The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.

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medical Class II
2026-05-06

Philips North America recalls Philips SmartPath to dStream for 1.5T with MR Elastography (

The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.

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medical Class II
2026-06-17

Philips North America Llc recalls DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 71203

System was delivered without the required Seismic kit for Wall Stand VS2, which is designed to prevent damage and ensure stability of the Wall Stand VS2 during seismic events.

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medical Class II
2026-07-01

Philips North America Llc recalls Philips Avalon Fetal Monitor, FM20, Part number M2702A, Part

Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or permanent loss of speaker output.

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medical Class II
2026-07-01

Philips North America Llc recalls Philips Avalon Fetal Monitor, FM 30 Part numberM2703A

Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or permanent loss of speaker output.

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medical Class II
2026-07-01

Philips North America Llc recalls Philips Telemetry Monitor 5500 1.4 GHz. Model Number: 867232

Potential for device reset to default "NEW_DEVICE" state, which may lead to a to loss of device configuration and the equipment label, resulting in a failure to reconnect to the PIC iX central monitoring system.

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