FDA recall record

Toshiba American Medical Systems XARIO 100 TUS-X100 diagnostic ultrasound system recall — FDA Z-2708-2017

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…

Class IIclassification
Z-2708-2017official record ID
Jul 19, 2017report date

Recall record at a glance

Official recordZ-2708-2017
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmToshiba American Medical Systems Inc.
Report dateJul 19, 2017
Recall initiation dateMay 1, 2017
Quantity7 units
LocationTustin, CA, United States

Official product description

XARIO 100 TUS-X100 diagnostic ultrasound system

Why the product was recalled

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.

Distribution information

Nationwide Distribution

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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