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Simpleware ScanIPRecalls & reported problems across all models

Synopsys, Inc. · 3 models in the FDA device registry

Data updated Oct 16, 2026 from official FDA records · Editorial policy

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

We found 3 models of Simpleware ScanIP by Synopsys, Inc. in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.

1 FDA recall record name at least one of these models by its device identifier.

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

Simpleware ScanIP 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. Jun 4, 2021Terminated

    A issue (bug) has been identified with the interface and image software which could result in anatomical orientation tags/labels being displayed incorrectly. This could result in operator misunderstanding and errors during resampling or re-alignment of image data

    Z-2253-2021 · Root cause: Software Manufacturing/Software Deployment · names 3 of these models · Recall details · FDA record ↗

Simpleware ScanIP models

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

Other Synopsys, Inc. products

All Synopsys, Inc. devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page