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FDA Device recall Z-3317-2026

Upgrade to MR 7700

On 2026-10-07 the FDA classified a Class II recall of Upgrade to MR 7700 by Philips North America, citing when exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-3317-2026
ClassificationClass II
Statusongoing
Initiated2026-08-28
Published2026-10-07
Last updated2026-10-13 05:30 UTC
CompanyPhilips North America
DistributionUS

Product

Upgrade to MR 7700; Model number (REF): 782130; Software Versions: R11, R12 and R13;

Reason

When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced MR DICOM export is used in conjunction with third-party software for tractography (e.g. for mapping nerve fiber pathways in the brain), the software will not be able to correctly process the DTI data for reconstruction.

Identifiers

code_info
Model number (REF): 782130; UDI-DI: 00884838104402; Serial Numbers: 42002, 42030, 42037, 42066, 42104, 42151, 42163, 42…Model number (REF): 782130; UDI-DI: 00884838104402; Serial Numbers: 42002, 42030, 42037, 42066, 42104, 42151, 42163, 42164, 42211, 42219, 42248, 42376, 45001, 45007, 45043, 45044, 45052, 45179, 45236, 45263, 45552, 71060, 71262, 71279, 71406, 71532, 71565, 71580, 71616, 71907;

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-10-13 05:30 UTC. Current status: ongoing.

Other recalls by Philips North America

All Philips North America recalls

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3317-2026%22

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