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IntraSight Plus 797423Recalls & reported problems

Philips Image Guided Therapy Corporation · The IntraSight Plus is an interventional applications workspace. · Class 2

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
1

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier, 1 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, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

  1. Aug 6, 2026Open, Classified

    Software system may associate image data from one patient with another patient's record, potentially resulting in incorrect diagnosis or treatment.

    Z-3276-2026 · Root cause: Software Design Change · FDA record ↗

Other System, Imaging, Pulsed Echo, Ultrasonic devices

All System, Imaging, Pulsed Echo, Ultrasonic devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.