MR 7700Recalls & reported problems across all models

We found 3 models of MR 7700 by Philips Medical Systems Nederland B.V. in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.

2 FDA recall records name at least one of these models by its device identifier, 2 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

MR 7700 recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

1. Aug 28, 2026Open, Classified

   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.

   Z-3315-2026 · Root cause: Software design · names 2 of these models · Recall details · FDA record ↗

2. Aug 28, 2026Open, Classified

   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.

   Z-3313-2026 · Root cause: Software design · Recall details · FDA record ↗

MR 7700 models

3 models, most reported first. Each model has its own page with its reports, recalls and device details.

• MR 7700

  System, Nuclear Magnetic Resonance Imaging
  1 recall0 reports
• MR 7700 SmartPath to MR 7700

  System, Nuclear Magnetic Resonance Imaging
  1 recall0 reports
• MR 7700 SmartPath to MR 7700

  System, Nuclear Magnetic Resonance Imaging
  1 recall0 reports

Other Philips Medical Systems Nederland B.V. products

• Allura Xper FD19 models · 15,187 reports · 84 recalls
• Azurion22 models · 9,199 reports · 71 recalls
• Ingenia54 models · 479 reports · 138 recalls
• IntelliSpace Cardiovascular11 models · 439 reports · 3 recalls
• MR 7000 Series2 models · 4 reports · 11 recalls
• Dynamic Coronary Roadmap3 models · 10 reports · 9 recalls
• MR 5000 Series3 models · 11 reports · 8 recalls
• Brilliance iCT2 models · 9 reports · 8 recalls