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Toshiba American Medical Systems Inc recalls APLIO 500 TUS-A500 diagnostic ultrasound system
Recalled July 19, 2017 · FDA recall Z-2711-2017 · Toshiba American Medical Systems
Hazard
When Continuous Trace method is used as the tracing method on Spectral Doppler in velocity trace measurement, an incorrect value may be displayed in the ultrasound systems and in the ultrasound workstations listed below. · FDA Class II
Units
307 units
Sold at
Nationwide Distribution
Description
When Continuous Trace method is used as the tracing method on Spectral Doppler in velocity trace measurement, an incorrect value may be displayed in the ultrasound systems and in the ultrasound workstations listed below.
Product
APLIO 500 TUS-A500 diagnostic ultrasound system
Manufacturer(s)
Toshiba American Medical Systems Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →