Ultrasound System SONIMAGE HS1Recalls & reported problems across all models
Konica Minolta, Inc. · 2 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 1
We found 2 models of Ultrasound System SONIMAGE HS1 by Konica Minolta, 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
Ultrasound System SONIMAGE HS1 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.
- Apr 24, 2017Class IITerminated
The Doppler velocity measurement on the Sonimage HS1 ultrasound system is not accurate.
Z-2769-2017 · Root cause: Software design · names 2 of these models · Recall details · FDA record ↗
Ultrasound System SONIMAGE HS1 models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Ultrasound System SONIMAGE HS1 A7APSystem, Imaging, Pulsed Doppler, Ultrasonic1 recall0 reports
- Ultrasound System SONIMAGE HS1 A9RPSystem, Imaging, Pulsed Doppler, Ultrasonic1 recall0 reports
Other Konica Minolta, Inc. products
All Konica Minolta, Inc. devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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