Philips North America

Philips North America: 3 recalls listed since April 2026 across FDA.

By year

Ingenia Blue Seal SE and Blue Seal XE export incorrect diffusion data when using Enhanced MR Dicom format.

Moderate riskFDASep 25, 2026Software defect

Medical devices

Philips Patient Information Center iX may freeze and become unresponsive due to software malfunction.

Moderate riskFDASep 11, 2026Software defect

Philips Achieva 1.5T with MR Elastography may display stiffness values that are too small.

Moderate riskFDAApr 27, 2026Software defect