Toshiba American Med Sys Inc Aplio Diagnostic Ultrasound System (SSA-700A and SSA-770A) with software version 6.0er001 and 6.0er002 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Aplio Diagnostic Ultrasound System (SSA-700A and SSA-770A) with software version 6.0er001 and 6.0er002
Brand
Toshiba American Med Sys Inc
Lot Codes / Batch Numbers
Software versions 6.0er001 and 002
Products Sold
Software versions 6.0er001 and 002
Toshiba American Med Sys Inc is recalling Aplio Diagnostic Ultrasound System (SSA-700A and SSA-770A) with software version 6.0er001 and 6.0er0 due to If the measurement mode is started from the Doppler mode and then the sweep speed setting is changed by the assigned user function, the measurement o. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
If the measurement mode is started from the Doppler mode and then the sweep speed setting is changed by the assigned user function, the measurement of the time direction results don't correspond to the actual values.
Recommended Action
Per FDA guidance
Firm issued a recall letter which provided a procedural workaround, a software patch will be installed during routine service visits.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026