HS70A Diagnostic Ultrasound System USS-HS7AL4L/WWRecalls & reported problems

Summary

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

2 FDA recall records name this device's 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, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Recalls naming this device

1. Jul 15, 2020Class IITerminated

   There are potential issues related to the operational state of the scanner, specifically for transport and inadvertent system shutdowns. There could be a possibility of potential delay in patient treatment if proper use instructions are not followed.

   Z-2772-2020 · Root cause: Device Design · Recall details · FDA record ↗

2. Jul 25, 2019Class IITerminated

   There is a potential for probes overheating when decreasing the Doppler SV (Sample Volume) size value set by the user in the Doppler Only mode.

   Z-2275-2019 · Root cause: Software design · Recall details · FDA record ↗